LMG Compliance Portal
Cosmetic Registration Navigator
Find out whether your cosmetic establishment requires FDA MoCRA facility registration and whether your products require listing — including private label distributors and foreign facilities.
MoCRA Product Code Builder
Identify the correct FDA MoCRA product category code for your cosmetic product. Essential for MoCRA facility registration and product listing submissions.
Cosmetic vs. Drug Classifier
Determine whether your product is regulated as a cosmetic, an OTC drug, or both — based on FDA's official classification criteria under the FD&C Act.
Cosmetic Label Scanner
Scan your cosmetic label against FDA and MoCRA requirements. Instantly identify compliance risks across product identity, ingredient declaration, responsible person information, and more.
Food Facility Registration Navigator
Determine whether your facility must register with FDA under FSMA and the Bioterrorism Act. Covers manufacturers, importers, exporters, warehouses, corporate offices, and more.
LACF / AF Requirement Navigator
Determine if your food product requires FDA Food Canning Establishment (FCE) registration and Scheduled Identifier (SID) filing under 21 CFR Part 108.
Food Label Scanner
Check whether your food label meets FDA requirements under 21 CFR Part 101 — covering identity, net quantity, ingredients, Nutrition Facts, allergens, and claims. Get an instant compliance score.
Device Classification Finder
Answer 4 questions to determine whether your medical device is Class I, II, or III and whether a 510(k) premarket notification or PMA is required.
Medical Device Label Scanner
Scan your medical device label against FDA requirements under 21 CFR Part 801. Instantly identify risks across device identity, UDI, intended use, warnings, and Rx/OTC status.
Instantly validate your NDC number format and decode the labeler, product, and package code segments. Checks 4-4-2, 5-3-2, and 5-4-1 formats.
OMUFA Fee Navigator
Determine whether your drug establishment owes OTC Monograph User Fees (OMUFA) under the CARES Act 2020. Includes FY2025 fee rates and key exemptions.
Drug Label Scanner
Scan your drug label against FDA requirements under 21 CFR Part 201. Instantly identify risks across active ingredients, Drug Facts panel, warnings, directions, and allergen declarations.
FDA Registration Fee Estimator
Select your product category and required services to get an instant itemized fee estimate. LMG service fees have not changed since 2009.