Home NDC 59316-102 BIOFREEZE
Product NDC 59316-102
11-digit product format 593160102
Labeler code 59316
Product ID 59316-102_51b44481-a7ad-8a46-e063-6294a90aefda
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler Reckitt Benckiser LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-01-03
Substance MENTHOL, UNSPECIFIED FORM
Active strength 40 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base BIOFREEZE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 415974 Internal RxNorm lookup 1111683 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59316-102 BIOFREEZE (MENTHOL) GEL [RB HEALTH (US) LLC] 34 Current NDC, Legacy NDC, 16 package rows 20231114_83d5c2f2-2413-4d28-83b2-0808d0917b4d.zip 59316-102 BIOFREEZE (MENTHOL) GEL [PERFORMANCE HEALTH, LLC] 1 Current NDC, Legacy NDC, 1 package rows 20181108_f0c4d165-a242-4fb5-b2de-d64a825a29e9.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 85 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PROINNATE Numbing Cream MENTHOL Guangzhou Haishi Biological Technology Co., Ltd. 39688b2b-c1fe-cd86-e063-6394a90a5345 2025-07-16 Warnings Exact identifier application number: M017 Methyl Salicylate METHYL SALICYLATE ViolaCare, Inc. 8f0ba6e7-8aa4-443e-99ae-a255085ddfec 2025-07-15 Warnings Exact identifier application number: M017 TopCare Hydrocortisone Intensive Healing Formula HYDROCORTISONE Topco Associates LLC 7daafc44-e2a4-4f1b-bfca-3309a8e9a920 2025-07-15 Warnings Exact identifier application number: M017 Hydrocortisone Plus 12 Moisturizers HYDROCORTISONE TARGET Corporation 72c3889c-b743-4728-a315-6e4063e00200 2025-07-15 Warnings Exact identifier application number: M017 Shopko Hydrocortisone Maximum Strength HYDROCORTISONE Shopko Stores Operating Co., LLC 0431a6af-4c9a-4bbd-a535-cba31a5e53cc 2025-07-15 Warnings Exact identifier application number: M017 Freds Hydrocortisone with Aloe HYDROCORTISONE FRED'S, INC. 076503bf-8238-4739-bb1c-c385e72f8a96 2025-07-15 Warnings Exact identifier application number: M017 Shopko Hydrocortisone HYDROCORTISONE Shopko Stores Operating Co., LLC 92bcbde3-401a-4301-854e-c352852317d6 2025-07-15 Warnings Exact identifier application number: M017 TopCare Hydrocortisone HYDROCORTISONE Topco Associates LLC bd3585fa-3b48-49b7-8ad1-749bf1e31ed5 2025-07-15 Warnings Exact identifier application number: M017 Methyl Salicylate 25% Pain Relieving METHYL SALICYLATE Puretek Corporation 376797ff-cf13-a3c6-e063-6394a90a9de1 2025-07-15 Warnings Exact identifier application number: M017 TIGER BALM PAIN RELIEVING CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. 440e97bc-bd97-4733-9955-643b18e7fb18 2025-07-15 Warnings Exact identifier application number: M017 Tiger Balm Pain Relieving Hydrogel Large CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. 064d04ca-184d-492b-867c-beaa165ab3e0 2025-07-14 Warnings Exact identifier application number: M017 Methyl Salicylate 25% Cream METHYL SALICYLATE Medcore LLC 143f76bf-2de4-466a-8a6b-d6ab6314a2c3 2025-07-14 Warnings Exact identifier application number: M017 BLUESPRING Doctors Pain Formula Pain Relief MENTHOL ACA MANAGEMENT LLC 98f3f719-792f-4a93-95b1-90072e0f8bf4 2025-07-14 Warnings Exact identifier application number: M017 Shopko Anti-Itch DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Shopko Stores Operating Co., LLC 130119eb-b87e-4a07-8d2a-317369bfa541 2025-07-14 Warnings Exact identifier application number: M017 Equate Hydrocortisone Intensive Healing Formula HYDROCORTISONE Wal-Mart Stores Inc. 635b49c4-54d2-4b6d-bee8-851fc2c7ca9c 2025-07-14 Warnings Exact identifier application number: M017 ULTRA STRENGTH ZHENG GU SHUI MENTHOL AND CAMPHOR GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD 53397663-044d-4e48-989b-2c6257af5f84 2025-07-14 Warnings, Adverse reactions Exact identifier application number: M017 TIGER BALM PAIN RELIEVING HYDROGEL CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. cb60037f-bceb-4090-a5e4-bdda0cbf9f5c 2025-07-14 Warnings Exact identifier application number: M017 Avedana Hydrocortisone Cream with Aloe HYDROCORTISONE Unipack LLC 2a55c426-39b4-4d94-b6b4-6c548c9685e9 2025-07-13 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE ACETATE Rite Aid Corporation cb6e0bed-2ea1-49d2-89e7-2554e7565b74 2025-07-11 Warnings Exact identifier application number: M017 QUALITY CHOICE Maximum Strength Lidocaine Pain Relief Roll On LIDOCAINE HYDROCHLORIDE CHAIN DRUG MARKETING ASSOCIATION 7b3ff4c1-0b60-4f7a-8aa4-c84b7c7137c4 2025-07-11 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59316-102-10 59316010210 5 mL in 1 BOTTLE (59316-102-10) 5 ml 2012-01-03 0000-00-00 No No Current 59316-102-11 59316010211 3 mL in 1 BOTTLE (59316-102-11) 3 ml 2012-01-03 0000-00-00 No No Current 59316-102-12 59316010212 89 mL in 1 BOTTLE (59316-102-12) 89 ml 2016-09-19 0000-00-00 No No Current 59316-102-15 59316010215 89 mL in 1 BOTTLE, WITH APPLICATOR 89 ml Historical 59316-102-16 59316010216 89 mL in 1 BOTTLE, WITH APPLICATOR 89 ml Historical 59316-102-20 59316010220 118 mL in 1 BOTTLE (59316-102-20) 118 ml 2012-01-03 0000-00-00 No No Current 59316-102-25 59316010225 118 mL in 1 BOTTLE, WITH APPLICATOR (59316-102-25) 118 ml 2012-01-03 2021-12-31 No No Current 59316-102-28 59316010228 237 mL in 1 BOTTLE (59316-102-28) 237 ml 2016-09-19 0000-00-00 No No Current 59316-102-30 59316010230 473 mL in 1 BOTTLE (59316-102-30) 473 ml 2012-01-03 0000-00-00 No No Current 59316-102-40 59316010240 946 mL in 1 BOTTLE (59316-102-40) 946 ml 2012-01-03 0000-00-00 No No Current 59316-102-50 59316010250 3785 mL in 1 CONTAINER (59316-102-50) 3785 ml 2012-01-03 0000-00-00 No No Current 59316-102-80 59316010280 44 mL in 1 TUBE (59316-102-80) 44 ml 2018-11-02 0000-00-00 No No Current 59316-102-90 59316010290 100 BOTTLE in 1 CARTON (59316-102-90) / 5 mL in 1 BOTTLE (59316-102-10) 100 bottle 2012-01-03 0000-00-00 No No Current 59316-102-91 59316010291 10 BOTTLE in 1 CARTON (59316-102-91) > 3 mL in 1 BOTTLE (59316-102-11) 10 bottle 2012-01-03 0000-00-00 No No Current 59316-102-92 59316010292 16 BOTTLE in 1 CARTON (59316-102-92) > 3 mL in 1 BOTTLE (59316-102-11) 16 bottle 2012-01-03 0000-00-00 No No Current 59316-102-98 59316010298 30 mL in 1 BOTTLE (59316-102-98) 30 ml 2012-01-03 0000-00-00 No No Current