Alcohol Prep

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: Alcohol Prep
Generic name: ISOPROPYL ALCOHOL
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 39b20f1b-8d2f-4fa0-8cb9-10cad408e064
SPL ID: 461840ed-4af3-c2fb-e063-6294a90ab572
Version: 22
Effective date: 2025-12-16
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:52

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 · 39 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Alcohol Prep	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-121-18	openfda.package_ndc
ndc	package	67777-121-12	openfda.package_ndc
ndc	package	67777-121-26	openfda.package_ndc
ndc	package	67777-121-11	openfda.package_ndc
ndc	package	67777-121-22	openfda.package_ndc
ndc	package	67777-121-24	openfda.package_ndc
ndc	package	67777-121-19	openfda.package_ndc
ndc	package	67777-121-27	openfda.package_ndc
ndc	package	67777-121-13	openfda.package_ndc
ndc	package	67777-121-23	openfda.package_ndc
ndc	package	67777-121-16	openfda.package_ndc
ndc	package	67777-121-21	openfda.package_ndc
ndc	package	67777-121-17	openfda.package_ndc
ndc	package	67777-121-20	openfda.package_ndc
ndc	package	67777-121-14	openfda.package_ndc
ndc	product	67777-121	openfda.product_ndc
ndc11	package	67777012127	derived:openfda.package_ndc
ndc11	package	67777012117	derived:openfda.package_ndc
ndc11	package	67777012113	derived:openfda.package_ndc
ndc11	package	67777012120	derived:openfda.package_ndc
ndc11	package	67777012126	derived:openfda.package_ndc
ndc11	package	67777012116	derived:openfda.package_ndc
ndc11	package	67777012112	derived:openfda.package_ndc
ndc11	package	67777012121	derived:openfda.package_ndc
ndc11	package	67777012114	derived:openfda.package_ndc
ndc11	package	67777012123	derived:openfda.package_ndc
ndc11	package	67777012118	derived:openfda.package_ndc
ndc11	package	67777012124	derived:openfda.package_ndc
ndc11	package	67777012122	derived:openfda.package_ndc
ndc11	package	67777012119	derived:openfda.package_ndc
ndc11	package	67777012111	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		461840ed-4af3-c2fb-e063-6294a90ab572	id
spl set id		39b20f1b-8d2f-4fa0-8cb9-10cad408e064	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 · 1 matching rows.

warnings

Warnings For External Use only Flammable. Keep away from fire or flame. Do not use • In the eyes or over large areas of the body • Longer than 1 week unless directed by a doctor • With electrocautery procedures Ask a doctor before use if you have Deep or puncture wounds, animal bites, or serious burns. Stop use and ask a doctor if Condition persists for more than 72 hours or gets worse. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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