Home NDC 54622-122-01 Pacific Blue Ultra Foaming
Product NDC 54622-122
Requested package NDC 54622-122-01
11-digit product format 546220122
Labeler code 54622
Product ID 54622-122_2c631dee-f120-58af-e063-6394a90ac821
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 2021-06-11
Substance ALCOHOL
Active strength 70 mg/mL
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 54622-122 54622-122-01 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 54622-122 54622-122-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 Pacific Blue Ultra Foaming
Brand name suffix Fragrance Free
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mg/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 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 54622-122-01 Pacific Blue Ultra FoamingFragrance Free 1000 mL in 1 BOTTLE, DISPENSING SOLUTION 1000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54622-122 PACIFIC BLUE ULTRA FOAMING FRAGRANCE FREE (ETHYL ALCOHOL) SOLUTION [GEORGIA-PACIFIC CONSUMER PRODUCTS LP] 4 Current NDC, Legacy NDC, 1 package rows 20250124_c4840ac2-978c-3aac-e053-2995a90ad312.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 54622-122-01 54622012201 1000 mL in 1 BOTTLE, DISPENSING (54622-122-01) 1000 ml 2021-06-11 0000-00-00 No No Current