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Product NDC
75981-370
Requested package NDC
75981-370-45
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage75981-37075981-370-45DDiscontinued by firm2026-08-11

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 dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage75981-37075981-370-45DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage75981-37075981-370-45EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

Finished product
Yes
Brand name base
Advanced
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
581662Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
68eca241-acce-4f12-9643-bec9b14f53d0Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75981-370-16Advanced59 mL in 1 BOTTLE, PLASTICGEL5919
75981-370-34Advanced236 mL in 1 BOTTLE, PLASTICGEL23619
75981-370-45Advanced946 mL in 1 BOTTLE, PLASTICGEL94619

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
ALCOHOLACTIVE MOIETY3K9958V90MADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
.ALPHA.-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L0ADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)INACTIVE INGREDIENT71DD5V995LADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
GLYCERYL CAPRYLATE/CAPRATEINACTIVE INGREDIENTG7515SW10NADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
SULISOBENZONEINACTIVE INGREDIENT1W6L629B4KADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1
WATERINACTIVE INGREDIENT059QF0KO0RADVANCED (ETHYL ALCOHOL) GEL [GEISS, DESTIN + DUNN, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75981-370ADVANCED (ETHYL ALCOHOL) GEL [PERRIGO DIRECT, INC]16Current NDC, Legacy NDC, 3 package rows20240920_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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AdvancedETHYL ALCOHOLPerrigo Direct, Inc68eca241-acce-4f12-9643-bec9b14f53d02026-02-19Warnings, Adverse reactionsExact identifier
ndc (package): 75981-370-45
ndc (product): 75981-370
ndc11 (package): 75981037045

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN68eca241-acce-4f12-9643-bec9b14f53d019
581662ethanol 0.7 ML/ML Topical GelSCD68eca241-acce-4f12-9643-bec9b14f53d019
581662ethanol 70 % Topical GelSY68eca241-acce-4f12-9643-bec9b14f53d019
581662ethyl alcohol 70 % Topical GelSY68eca241-acce-4f12-9643-bec9b14f53d019

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75981-370-4575981037045946 mL in 1 BOTTLE, PLASTIC (75981-370-45) 946 ml2012-09-200000-00-00NoNoCurrent