Home NDC 11673-261 Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On
Product NDC 11673-261
11-digit product format 116730261
Labeler code 11673
Product ID 11673-261_0f95e27d-e2be-917a-e063-6294a90a5709
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler TARGET CORPORATION
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-21
Substance MENTHOL, UNSPECIFIED FORM
Active strength 40 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On
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 · 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-261-03 Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On 89 mL in 1 BOTTLE, WITH APPLICATOR GEL 89 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-261 TARGET UP AND UP PAIN RELIEF MENTHOL TOPICAL ANALGESIC ROLL-ON (MENTHOL) GEL [TARGET CORPORATION] 1 Current NDC, 1 package rows 20240124_0f95fc55-8665-9e89-e063-6394a90a7891.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 48 of 153 · 3,057 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 11673-261-03 11673026103 89 mL in 1 BOTTLE, WITH APPLICATOR (11673-261-03) 89 ml 2023-11-21 No No Current