AUM Alcohol Pad

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: AUM Alcohol Pad
Generic name: ALCOHOL PAD
Manufacturer: SLV PHARMACEUTICALS LLC DBA AUM PHARMACEUTICALS
Product type: HUMAN OTC DRUG
SPL set ID: 632da1b7-70bb-467d-81b2-39536f9fff3c
SPL ID: f149cd67-a3ab-43a5-b2ed-725eb8d12413
Version: 1
Effective date: 2025-02-26
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:08

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		AUM Alcohol Pad	openfda.brand_name
generic name		ALCOHOL PAD	openfda.generic_name
manufacturer name		SLV PHARMACEUTICALS LLC DBA AUM PHARMACEUTICALS	openfda.manufacturer_name
ndc	package	73317-8801-1	openfda.package_ndc
ndc	product	73317-8801	openfda.product_ndc
ndc11	package	73317880101	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		f149cd67-a3ab-43a5-b2ed-725eb8d12413	id
spl set id		632da1b7-70bb-467d-81b2-39536f9fff3c	set_id
unii		ND2M416302	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For External Use Only Avoid contact with the eyes If contact occurs, flush eyes with water Flammable, keep away from fire or flame. Do Not Use With electrocautery prodedures In the eyes Stop Use and ask a doctor if Irritation and redness develops If condition persists for more than 72 hours, consult a physician Discontinue use and consult a healthcare practitioner if Irritation develops Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away

warnings and cautions

Flammable, keep away from fire or flame.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.