Home NDC 55910-883-01 DG Health Cold n Hot Pain Relieving
Product NDC 55910-883
Requested package NDC 55910-883-01
11-digit product format 559100883
Labeler code 55910
Product ID 55910-883_c4b075fb-db59-4239-aede-60854bc6d1f8
Type HUMAN OTC DRUG
Nonproprietary name menthol, unspecified form
Dosage form LIQUID
Route TOPICAL
Labeler Dolgencorp Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-12-27
Substance MENTHOL, UNSPECIFIED FORM
Active strength 160 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 DG Health Cold n Hot Pain Relieving
Brand name suffix Topical Analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 160 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 866084 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 55910-883-01 DG Health Cold n Hot Pain RelievingTopical Analgesic 74 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 74 4 55910-883-01 DG Health Cold n Hot Pain RelievingTopical Analgesic 1 in 1 CARTON LIQUID 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-883 DG HEALTH COLD N HOT PAIN RELIEVING TOPICAL ANALGESIC (MENTHOL, UNSPECIFIED FORM) LIQUID [DOLGENCORP INC] 3 Current NDC, Legacy NDC, 2 package rows 20241101_8fe13b85-ab74-42f8-a664-d3d2959921ac.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 97 of 151 · 3,010 matching rows.
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 55910-883-01 55910088301 1 BOTTLE, WITH APPLICATOR in 1 CARTON (55910-883-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR 2019-12-27 0000-00-00 No No Current