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Regulatory compliance

Checks against industry and government rules to flag violations before anything goes live

‍

Best practices

Channel-specific guidance to reduce rejections and lift engagement

Creative compliance

Claim wording, imagery, targeting and audience suitability

Platform & channel policies

Stay aligned with evolving ad and content policies

Accessibility 
& transparency

Plain language, inclusivity, and readability checks so content is clear, accessible, and trustworthy

Brand consistency

Upload your internal rules and style guides to enforce voice, terminology, and visual identity across every asset

Regulatory compliance

Checks against industry and government rules to flag violations before anything goes live

Best practices

Channel-specific guidance to reduce rejections and lift engagement

Creative compliance

Claim wording, imagery, targeting and audience suitability

Platforma and channel policies

Stay aligned with evolving ad and content policies

Accessibility & transparency

Plain language, inclusivity, and readability checks so content is clear, accessible, and trustworthy

Brand consistency

Upload your internal rules and style guides to enforce voice, terminology, and visual identity across every asset

Find checks* that fit your needs

*Check is a set of rules grouped under one topic that checks whether content follows the requirements,
guidelines, or best practices related to that topic.

Food & Beverage Labeling – Nutrition Facts Panel Requirements
FDA
Establishes mandatory nutrition labeling requirements for packaged foods, including standardized format, content, serving sizes, and nutrient declarations.
December 5, 2025
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Food & Beverage Labeling – Nutrition Facts Panel Requirements
FDA
US
December 5, 2025
What it checks
•
Nutrition Facts Panel Format – Requires standardized nutrition label displaying serving size, calories, and nutrients in prescribed order with specific typography and spacing requirements.
•
Serving Size Standards – Establishes reference amounts customarily consumed (RACCs) and requires serving sizes to reflect typical consumption patterns, with specific calculation methods for different food categories.
•
Nutrient Declarations – Mandates disclosure of total fat, saturated fat, trans fat, cholesterol, sodium, carbohydrates, fiber, sugars, added sugars, protein, and certain vitamins/minerals with daily value percentages.
Where it applies
Industries:
Food & Beverage, Pharma & Healthcare
Content types:
Packaging & Labeling, Product Descriptions, Retail & In-Store, Legal & Regulatory
Channels / platforms:
Packaging, Retail, Ecommerce, Web
Cosmetic Labeling – FDA Requirements & Standards
FDA
Establishes FDA standards for cosmetic labeling including ingredient disclosure, package form requirements, and misbranding provisions.
December 5, 2025
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Cosmetic Labeling – FDA Requirements & Standards
FDA
US
December 5, 2025
What it checks
•
Ingredient Declaration – Requires cosmetics to list all ingredients in descending order of predominance using established INCI names, with specific font size and placement requirements on packaging.
•
Misbranding Prevention – Prohibits false or misleading representations, requires accurate ingredient naming, and establishes clear standards for sunscreen terminology to avoid consumer confusion.
•
Package Labeling – Mandates principal display panel standards including identity statements, net quantity declarations, and manufacturer information with specific prominence and conspicuousness rules.
Where it applies
Industries:
Pharma & Healthcare, Consumer Goods (CPG)
Content types:
Packaging & Labeling, Product Descriptions, Retail & In-Store
Channels / platforms:
Retail, Packaging, Ecommerce, Web
OTC Drug Products – Labeling, Manufacturing & Safety Standards
FDA
Establishes general recognition standards for over-the-counter drugs, covering manufacturing practices, labeling requirements, and safety protocols.
December 5, 2025
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OTC Drug Products – Labeling, Manufacturing & Safety Standards
FDA
US
December 5, 2025
What it checks
•
Manufacturing Compliance – Products must be manufactured in compliance with current good manufacturing practices (cGMP) as established by 21 CFR parts 210 and 211, with proper establishment registration and drug product listing.
•
Safety Standards – Requires pregnancy-nursing warnings, imprinting of solid oral dosage forms, adherence to monograph conditions, and compliance with ingredient safety and effectiveness criteria established through OTC drug review.
•
Labeling Requirements – Products must comply with Federal Food, Drug, and Cosmetic Act chapter V labeling standards, including format and content requirements in §201.66, with proper drug category identification and warnings.
Where it applies
Industries:
Pharma & Healthcare, Consumer Goods (CPG)
Content types:
Packaging & Labeling, Product Descriptions, Legal & Regulatory
Channels / platforms:
Packaging, Retail, Ecommerce, Web
Prescription Drug Advertising – Labeling & Disclosure Standards
FDA
Regulates prescription drug advertising to ensure proper ingredient disclosure, established name usage, and balanced risk/benefit presentation.
December 5, 2025
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Prescription Drug Advertising – Labeling & Disclosure Standards
FDA
US
December 5, 2025
What it checks
•
Ingredient Disclosure – Requires established names to accompany proprietary names in advertising, with specific type size ratios (at least half as large) and clear presentation standards to prevent confusion.
•
Fair Balance Standard – Prohibits false or misleading claims by requiring truthful presentation of both benefits and risks, with equal prominence given to safety information alongside efficacy claims.
•
Brief Summary Requirements – Mandates inclusion of side effects, contraindications, and effectiveness information in a balanced manner, with specific formatting rules for print, broadcast, and digital media.
Where it applies
Industries:
Pharma & Healthcare
Content types:
Ads & Social Media, Print Materials, Video & Multimedia, Web & SEO Content
Channels / platforms:
Print, TV, Radio, Web, Email
Prescription Drug Labeling – Content & Format Requirements
FDA
Establishes comprehensive labeling standards for prescription drugs including content, format, warnings, and required disclosures.
December 5, 2025
Learn more
Close
Prescription Drug Labeling – Content & Format Requirements
FDA
US
December 5, 2025
What it checks
•
Content Requirements – Mandates specific sections including indications, dosage, contraindications, warnings, adverse reactions, and clinical pharmacology with standardized formatting and placement.
•
Format Standards – Specifies labeling structure with principal display panel, statement of identity, net quantity, bar code requirements, and expiration date placement to ensure consistency.
•
Warning & Safety Disclosures – Requires prominent boxed warnings for serious risks, pregnancy/nursing warnings, pediatric use statements, and specific warnings for sulfites and phenylalanine content.
Where it applies
Industries:
Pharma & Healthcare
Content types:
Packaging & Labeling, Legal & Regulatory, Product Descriptions
Channels / platforms:
Packaging, Retail, Web
Food Labeling & Naming Standards – Common or Usual Names for Nonstandardized Foods (21 CFR Part 102)
FDA
Establishes naming standards for nonstandardized foods, requiring accurate identification, characterizing ingredient disclosure, and consistent terminology.
December 5, 2025
Learn more
Close
Food Labeling & Naming Standards – Common or Usual Names for Nonstandardized Foods (21 CFR Part 102)
FDA
US
December 5, 2025
What it checks
•
Naming Requirements – Common or usual names must accurately identify the food's basic nature in simple terms, be uniform across identical products, and distinguish the food from different products (e.g., 'onion rings made from diced onion').
•
Presence/Absence Statements – Must disclose presence, absence, or need to add characterizing ingredients when material to price or acceptance, with specific requirements for imitation products and fabricated foods (e.g., 'fish sticks made from minced fish').
•
Characterizing Ingredient Disclosure – Requires percentage declaration of characterizing ingredients when proportion affects price or consumer acceptance, displayed in boldface type at specific minimum heights (1/16 inch for ≤5 sq. in. panels, 1/8 inch for larger panels).
Where it applies
Industries:
Food & Beverage, Consumer Goods (CPG)
Content types:
Packaging & Labeling, Product Descriptions
Channels / platforms:
Packaging, Retail, Ecommerce

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auto-updating Inspectors
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Explore our detailed FAQ section
for in-depth answers and insights
How does GetGenAI stay up to date with regulations?
GetGenAI connects directly to regulatory databases and trusted sources through APIs, so our Inspectors update in real time as laws, advertising codes, or platform policies change — no manual tracking or revalidation needed.
Can I add my own rules or brand guidelines?
Yes. You can upload internal rules — like brand tone, claim wording, or style guides — and GetGenAI will turn them into private Checks for your team.
What do Check results look like?
You’ll see what’s wrong or risky, why it matters, and how to fix it — often with a one-click option to apply the change automatically.
What are GetGenAI Checks?
Checks are smart rule sets built for specific needs — from industry regulations to creative best practices and brand voice. Each one reviews your content through a focused lens, like “FDA rules for health ads” or “tone and readability for SEO.”
Can I run multiple Checks at once?
Yes. Most teams combine several — for example, Regulatory + Creative + Brand Consistency — to cover all angles in one quick review.
How do I choose which Checks to use?
You can select Checks based on your industry, content type, and region, but we’ll also help you choose the right mix during your demo — tailoring them to your brand, workflows, and compliance needs.
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