Home NDC 54622-120 EnMotion Foam Hand Sanitizer
Product NDC 54622-120
11-digit product format 546220120
Labeler code 54622
Product ID 54622-120_2c62e697-63c2-a7a8-e063-6294a90a6607
Type HUMAN OTC DRUG
Nonproprietary name Ethyl alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Georgia-Pacific Consumer Products LP
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-25
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 54622-120-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 54622-120-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 54622-120-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 54622-120-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 54622-120-01 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 54622-120-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
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 Hand Sanitizer
Listing expiration 2026-12-31 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54622-120-01 EnMotion Foam Hand Sanitizer 1000 mL in 1 BAG LIQUID 1000 6 54622-120-01 EnMotion Foam Hand Sanitizer 2 in 1 BOX LIQUID 2 6 54622-120-02 EnMotion Foam Hand Sanitizer 1000 mL in 1 BOTTLE LIQUID 1000 6 54622-120-02 EnMotion Foam Hand Sanitizer 2 in 1 BOX LIQUID 2 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54622-120 ENMOTION FOAM HAND SANITIZER (ETHYL ALCOHOL) LIQUID [GEORGIA-PACIFIC CONSUMER PRODUCTS LP] 6 Current NDC, Legacy NDC, 4 package rows 20250124_639eb6c6-ff72-0291-e053-2a91aa0a3fb3.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 54622-120-01 54622012001 2 BAG in 1 BOX (54622-120-01) / 1000 mL in 1 BAG 2 bag 2018-01-25 0000-00-00 No No Current 54622-120-02 54622012002 2 BOTTLE in 1 BOX (54622-120-02) / 1000 mL in 1 BOTTLE 2 bottle 2018-01-25 0000-00-00 No No Current