Home NDC 75981-370 Advanced
Product NDC 75981-370
11-digit product format 759810370
Labeler code 75981
Product ID 75981-370_4b313078-2c80-5e87-e063-6394a90a1972
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler Perrigo Direct, Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-09-20
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 · 5 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 75981-370-45 D Discontinued by firm d630ba8d3edf…732f749b63fb…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 75981-370-45 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 75981-370-34 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 75981-370-16 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base Advanced
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 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 75981-370-16 Advanced 59 mL in 1 BOTTLE, PLASTIC GEL 59 19 75981-370-34 Advanced 236 mL in 1 BOTTLE, PLASTIC GEL 236 19 75981-370-45 Advanced 946 mL in 1 BOTTLE, PLASTIC GEL 946 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 ALCOHOL ACTIVE MOIETY 3K9958V90M ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) INACTIVE INGREDIENT 71DD5V995L ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 GLYCERYL CAPRYLATE/CAPRATE INACTIVE INGREDIENT G7515SW10N ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 SULISOBENZONE INACTIVE INGREDIENT 1W6L629B4K ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75981-370 ADVANCED (ETHYL ALCOHOL) GEL [PERRIGO DIRECT, INC] 16 Current NDC, Legacy NDC, 3 package rows 20240920_68eca241-acce-4f12-9643-bec9b14f53d0.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 75981-370-16 75981037016 59 mL in 1 BOTTLE, PLASTIC (75981-370-16) 59 ml 2012-09-20 0000-00-00 No No Current 75981-370-34 75981037034 236 mL in 1 BOTTLE, PLASTIC (75981-370-34) 236 ml 2012-09-20 0000-00-00 No No Current 75981-370-45 75981037045 946 mL in 1 BOTTLE, PLASTIC (75981-370-45) 946 ml 2012-09-20 0000-00-00 No No Current