Home NDC 79903-105 Equate Pain Relief Balm
Product NDC 79903-105
11-digit product format 799030105
Labeler code 79903
Product ID 79903-105_40aa5ef9-be48-5f8d-e063-6294a90a68a3
Type HUMAN OTC DRUG
Nonproprietary name Menthol 11%, Camphor 11% Ointment
Dosage form OINTMENT
Route TOPICAL
Labeler WALMART, INC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-01
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 110; 110 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 79903-105 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 79903-105 79903-105-18 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Equate Pain Relief Balm
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 110 mg/g CAMPHOR (SYNTHETIC) 110 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1089847 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79903-105-18 Equate Pain Relief Balm 1 in 1 CARTON OINTMENT 1 5 79903-105-18 Equate Pain Relief Balm 18 g in 1 BOTTLE, GLASS OINTMENT 18 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-105 EQUATE PAIN RELIEF BALM (MENTHOL 11%, CAMPHOR 11% OINTMENT) OINTMENT [WALMART, INC] 4 Current NDC, Legacy NDC, 2 package rows 20240317_d8ddf835-f008-ce1f-e053-2a95a90aa9b3.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 118 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tiger Balm METHYL SALICYLATE AND MENTHOL Haw Par Healthcare Ltd. 51293a06-5922-4072-ae14-afaba9c1b58e 2024-11-14 Warnings Exact identifier application number: M017 Tylenol Precise Warming Pain Relieving LIDOCAINE Kenvue Brands LLC 0c60b607-ade9-68f2-e063-6394a90a4025 2024-11-13 Warnings Exact identifier application number: M017 Tylenol Precise Pain Relieving LIDOCAINE Kenvue Brands LLC fc1e0451-8c84-729e-e053-6394a90aaba0 2024-11-13 Warnings Exact identifier application number: M017 Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE Kenvue Brands LLC 23222e54-d793-4d79-980e-550e32a95742 2024-11-13 Warnings Exact identifier application number: M017 TopCare Pain Relieving Roll-On Topical Analgesic MENTHOL, UNSPECIFIED FORM Topco Associates LLC 48589893-ca67-471d-88bc-92014295ab9f 2024-11-13 Warnings Exact identifier application number: M017 Benadryl Extra Strength Itch Stopping DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Kenvue Brands LLC a1c1b878-d58f-41ff-b7a8-477f28c52667 2024-11-12 Warnings Exact identifier application number: M017 Real Time Pain Relief Maxx Plus Topical Analgesic MENTHOL Real Time Products Inc. fc509a55-594d-4d44-87db-33286e937581 2024-11-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride LIDOCAINE HYDROCHLORIDE Acme United Corporation f1f051ad-7e82-9d1a-e053-2a95a90ac7d3 2024-11-12 Warnings Exact identifier application number: M017 HYDROCORTISONE HYDROCORTISONE ALLIED TRADE LINK LLC 26bc238d-3bda-0c29-e063-6394a90a35fb 2024-11-12 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Acme United Corporation fabcaa3b-d189-bd29-e053-6294a90ae86b 2024-11-12 Warnings Exact identifier application number: M017 ActivICE MENTHOL Medline Industries, LP 8414aea2-52b5-4221-e053-2a91aa0a622e 2024-11-12 Warnings Exact identifier application number: M017 Pain Relieving Gel-Patch LIDOCAINE Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 26c7116f-c86d-8752-e063-6294a90ab73f 2024-11-12 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Kroger Company fc1677f2-4078-4ebd-9c3b-86a29a35b489 2024-11-12 Warnings Exact identifier application number: M017 CVS Health Lidocaine Cream LIDOCAINE CVS Health ad950680-c03c-4fa5-aa7f-239a889cd097 2024-11-12 Warnings Exact identifier application number: M017 CVS Arthritis Pain Relief ARTHRITIS PAIN RELIEF CVS Health 575dd514-fd99-4e44-8fc8-52938f9abc26 2024-11-11 Warnings Exact identifier application number: M017 ThermaPatch (TM) Lidocaine Pain Relief Patch LIDOCAINE PAIN RELIEF PATCH Henan Enokon Medical Instrument Co., Ltd. 26769590-cd50-1b01-e063-6394a90a445c 2024-11-09 Warnings Exact identifier application number: M017 DG Health Cold Zone Pain Relieving Topical Analgesic MENTHOL, UNSPECIFIED FORM Dolgencorp Inc 22594ab8-9a4a-426f-aced-5c636620fa2c 2024-11-08 Warnings Exact identifier application number: M017 Peviderm Pramoxine Hydrocholride 1% PRAMOXINE HYDROCHLORIDE Stratus Pharmaceuticals Inc 680b40fa-1922-443a-a4b0-7c3f6a2b847d 2024-11-07 Warnings Exact identifier application number: M017 Meijer Analgesic with Aloe Topical Analgesic TROLAMINE SALICYLATE Meijer Distribution, Inc f6c1e09e-4c61-4c2a-87d7-b052ed36fcac 2024-11-07 Warnings Exact identifier application number: M017 Meijer Pain Relieving Balm Analgesic TROLAMINE SALICYLATE Meijer Distribution, Inc 1b7535cc-01ac-49f0-9889-dd14b254d4ae 2024-11-07 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 79903-105-18 79903010518 1 BOTTLE, GLASS in 1 CARTON (79903-105-18) / 18 g in 1 BOTTLE, GLASS 2022-04-01 0000-00-00 No No Current