Alcohol Prep 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: Alcohol Prep Pad
Generic name: ALCOHOL PREP PAD
Manufacturer: BioMed Resource Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 03be8a96-c163-0e22-e054-00144ff8d46c
SPL ID: 0e9d506d-8c0f-ab6b-e063-6294a90a5ab6
Version: 4
Effective date: 2024-01-10
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:07

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Alcohol Prep Pad	openfda.brand_name
generic name		ALCOHOL PREP PAD	openfda.generic_name
manufacturer name		BioMed Resource Inc.	openfda.manufacturer_name
ndc	package	69250-661-02	openfda.package_ndc
ndc	product	69250-661	openfda.product_ndc
ndc11	package	69250066102	derived:openfda.package_ndc
spl id		0e9d506d-8c0f-ab6b-e063-6294a90a5ab6	id
spl set id		03be8a96-c163-0e22-e054-00144ff8d46c	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

1. For external use only; 2. Flammable. Keep away from heat or flame; 3. Aviod to contact eyes. Flush throoughly with water in case of contact; 4. Stop use if irritation or redness develop; 5. Do not use with electrocautery procedures; Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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