Home NDC 54622-486-01 enMotion Foam
Product NDC 54622-486
Requested package NDC 54622-486-01
11-digit product format 546220486
Labeler code 54622
Product ID 54622-486_4a0372c0-7f0f-3e75-e063-6394a90aa9f1
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form SOLUTION
Route TOPICAL
Labeler Georgia-Pacific Consumer Products LP�
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-06-02
Substance ALCOHOL
Active strength 70 mL/100mL
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 enMotion Foam
Brand name suffix High Frequency Use
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
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 616805 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 54622-486-01 enMotion FoamHigh Frequency Use 1000 mL in 1 BOTTLE, DISPENSING SOLUTION 1000 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54622-486 ENMOTION FOAM HIGH FREQUENCY USE (ETHYL ALCOHOL) SOLUTION [GEORGIA PACIFIC CONSUMER PRODUCTS] 12 Current NDC, Legacy NDC, 1 package rows 20240920_e56f5a94-0be1-487b-ad95-c1fe74c824ee.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 54622-486-01 54622048601 1000 mL in 1 BOTTLE, DISPENSING (54622-486-01) 1000 ml 2016-06-09 0000-00-00 No No Current