Home NDC 79481-0088 meijer ROLL-ON Cold Therapy Pain Relieving
Product NDC 79481-0088
11-digit product format 794810088
Labeler code 79481
Product ID 79481-0088_f5c1ca8b-f929-4e6f-8f39-43acb5d53738
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route TOPICAL
Labeler Meijer Distribution, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-03
Substance MENTHOL, UNSPECIFIED FORM
Active strength 40 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 meijer ROLL-ON Cold Therapy Pain Relieving
Brand name suffix Topical analgesic
Listing expiration 2026-12-31 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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 415974 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79481-0088-1 meijer ROLL-ON Cold Therapy Pain RelievingTopical analgesic 74 mL in 1 BOTTLE, WITH APPLICATOR GEL 74 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0088 MEIJER ROLL-ON COLD THERAPY PAIN RELIEVING TOPICAL ANALGESIC (MENTHOL, UNSPECIFIED FORM) GEL [MEIJER DISTRIBUTION, INC] 1 Current NDC, 1 package rows 20240224_8bc3956b-b82d-4ed3-8bc3-db0078466bbc.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 109 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79481-0088-1 79481008801 74 mL in 1 BOTTLE, WITH APPLICATOR (79481-0088-1) 74 ml 2023-11-03 No No Current