Home NDC 53125-801-04 North Woods Derma Gel Clear
Product NDC 53125-801
Requested package NDC 53125-801-04
11-digit product format 531250801
Labeler code 53125
Product ID 53125-801_40a72db6-d505-3e66-e063-6294a90a6566
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler Superior Chemical Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-08-01
Substance ALCOHOL
Active strength .7 mL/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 North Woods Derma Gel Clear
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .7 mL/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581662 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 53125-801-04 North Woods Derma Gel Clear 3780 mL in 1 BOTTLE, PLASTIC GEL 3780 4 53125-801-09 North Woods Derma Gel Clear 500 mL in 1 BOTTLE, PUMP GEL 500 4 53125-801-29 North Woods Derma Gel Clear 1000 mL in 1 BAG GEL 1000 4 53125-801-57 North Woods Derma Gel Clear 550 mL in 1 BOTTLE, PUMP GEL 550 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53125-801 NORTH WOODS DERMA GEL CLEAR (ALCOHOL) GEL [SUPERIOR CHEMICAL CORPORATION] 3 Current NDC, Legacy NDC, 4 package rows 20241120_abbd099a-8d89-80a0-e053-2a95a90a24fc.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 1 of 1 · 1 matching rows.
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 53125-801-04 53125080104 3780 mL in 1 BOTTLE, PLASTIC (53125-801-04) 3780 ml 2019-08-01 0000-00-00 No No Current