Home NDC 59316-101 Biofreeze
Product NDC 59316-101
11-digit product format 593160101
Labeler code 59316
Product ID 59316-101_51b434c9-228b-2c05-e063-6394a90a1e94
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 2016-08-25
Substance MENTHOL, UNSPECIFIED FORM
Active strength 35 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 · 48 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 35 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 808955 Internal RxNorm lookup 1043451 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 59316-101 BIOFREEZE (MENTHOL) GEL [RB HEALTH (US) LLC] 42 Current NDC, Legacy NDC, 12 package rows 20241228_684faf63-5e44-4471-8384-e8fa7c0d842a.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 51 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Certain Dri Clinical Strength Prescription Protection Rollon CERTAIN DRI CLINICAL STRENGTH PRESCRIPTION PROTECTION ROLLON Clarion Brands LLC 46a1f92e-4411-3989-e063-6394a90a7038 2025-12-23 Warnings Exact identifier application number: M017 PREMIERES PAIN MENTHOL Premiere Enterprises 128bd1e7-e961-416c-933b-fbd146e3d386 2025-12-23 Warnings Exact identifier application number: M017 PREMIERES PAIN MENTHOL Premiere Enterprises 35ff19df-4cc4-4fce-bd30-d87d835e0e26 2025-12-23 Warnings Exact identifier application number: M017 Premieres Pain MENTHOL Premiere Enterprises 1f081913-6106-4d06-a37a-631f710dbacb 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. LIDOCAINE HCL, PHENOL Clarion Brands, LLC e1de73bb-917c-48d1-9a78-00c76edddb98 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE jr. PLUS Knee CAMPHOR, MENTHOL Clarion Brands, LLC 3ad8718d-ebf1-474f-8a91-48c78ab3b5c1 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr. Plus MENTHOL Clarion Brands, LLC fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR PLUS ULTRA STRENGTH PAIN MENTHOL Clarion Brands, LLC cf329707-d90a-29dd-f2c2-acfd5af614f3 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro Cream LIDOCAINE HCL, PHENOL Clarion Brands, LLC 17b3f1e6-5554-4f3e-b133-76ae8ffea919 2025-12-23 Warnings Exact identifier application number: M017 Absorbine Jr Pro No Mess Roll-on Plus LIDOCAINE HCL, PHENOL Clarion Brands, LLC a7172f17-1525-4738-b72c-92479c730af2 2025-12-23 Warnings Exact identifier application number: M017 ABSORBINE JR MENTHOL Clarion Brands, LLC d656e7f6-ca26-1873-6c11-08aa82091bb0 2025-12-23 Warnings Exact identifier application number: M017 Relief Recovery METHYL SALICYLATE Mayway Corporation 27afd45e-2dc5-d099-e063-6394a90ad2b7 2025-12-23 Warnings Exact identifier application number: M017 Mobility METHYL SALICYLATE Mayway Corporation 27af9d17-9c15-5e2a-e063-6394a90aeda5 2025-12-23 Warnings Exact identifier application number: M017 medlot pain relief gel patch LIDOCAINE Lotfancy, Inc. 3ce4af20-b227-5b98-e063-6394a90ab992 2025-12-23 Warnings Exact identifier application number: M017 Nizoral Scalp Itch Relief HYDROCORTISONE Kramer Laboratories dba59238-6beb-447e-8c4c-e4bc00fd2c20 2025-12-23 Warnings Exact identifier application number: M017 Salonpas LIDOCAINE Pain Relieving LIDOCAINE Hisamitsu America, Inc. 63911880-8194-4c7d-a72f-cab94761b2d7 2025-12-23 Warnings Exact identifier application number: M017 The Body Builders Cream MENTHOL Smart Cookie Solutions f803325e-eb86-4b9e-a401-0a91bdcd6389 2025-12-22 Warnings Exact identifier application number: M017 PROINNATE Numbing Cream LIDOCAINE,MENTHOL Guangdong Aimu Biological Technology Co., Ltd 46895ddb-0b9f-675e-e063-6394a90adf23 2025-12-22 Warnings Exact identifier application number: M017 Caring Mills Vaginal Anti-Itch Cream BENZOCAINE, RESORCINOL Veridian Healthcare f2362658-aea2-438e-a66c-738022e6e047 2025-12-22 Warnings Exact identifier application number: M017 HealthWise Pain Relieving Menthol Gel MENTHOL 2% Veridian Healthcare 396d0fd4-67be-4de1-8f0c-42c83dfe9120 2025-12-22 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 59316-101-10 59316010110 5 mL in 1 PACKET (59316-101-10) 5 ml 2016-08-25 0000-00-00 No No Current 59316-101-11 59316010111 30 mL in 1 BOTTLE (59316-101-11) 30 ml 2016-08-25 0000-00-00 No No Current 59316-101-12 59316010112 59 mL in 1 TUBE (59316-101-12) 59 ml 2016-08-25 0000-00-00 No No Current 59316-101-13 59316010113 59 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-13) 59 ml 2016-08-25 0000-00-00 No No Current 59316-101-15 59316010115 89 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-15) 89 ml 2016-08-25 0000-00-00 No No Current 59316-101-19 59316010119 3 mL in 1 PACKET (59316-101-19) 3 ml 2022-01-01 0000-00-00 No No Current 59316-101-20 59316010120 118 mL in 1 TUBE (59316-101-20) 118 ml 2016-08-25 0000-00-00 No No Current 59316-101-21 59316010121 81 mL in 1 TUBE 81 ml Historical 59316-101-25 59316010125 118 mL in 1 TUBE, WITH APPLICATOR (59316-101-25) 118 ml 2016-08-25 2021-12-31 No No Current 59316-101-30 59316010130 473 mL in 1 BOTTLE, PUMP (59316-101-30) 473 ml 2016-08-25 0000-00-00 No No Current 59316-101-40 59316010140 946 mL in 1 BOTTLE, PUMP (59316-101-40) 946 ml 2016-08-25 0000-00-00 No No Current 59316-101-50 59316010150 3785 mL in 1 BOTTLE, PUMP (59316-101-50) 3785 ml 2016-08-25 0000-00-00 No No Current