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: ISOPROPYL ALCOHOL
Manufacturer: Shandong Haiyan Medical Manufacture Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 1a117840-22d0-4a88-b1a6-e43162a444ab
SPL ID: da8c3af9-5d84-1c41-e053-2a95a90acc13
Version: 6
Effective date: 2022-03-19
Source export date: 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:03:52

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 2 · 67 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Alcohol Prep Pad	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Shandong Haiyan Medical Manufacture Co., Ltd.	openfda.manufacturer_name
ndc	package	42339-001-01	openfda.package_ndc
ndc	package	42339-001-11	openfda.package_ndc
ndc	package	42339-001-17	openfda.package_ndc
ndc	package	42339-001-23	openfda.package_ndc
ndc	package	42339-001-03	openfda.package_ndc
ndc	package	42339-001-08	openfda.package_ndc
ndc	package	42339-001-16	openfda.package_ndc
ndc	package	42339-001-12	openfda.package_ndc
ndc	package	42339-001-20	openfda.package_ndc
ndc	package	42339-001-09	openfda.package_ndc
ndc	package	42339-001-29	openfda.package_ndc
ndc	package	42339-001-05	openfda.package_ndc
ndc	package	42339-001-21	openfda.package_ndc
ndc	package	42339-001-26	openfda.package_ndc
ndc	package	42339-001-06	openfda.package_ndc
ndc	package	42339-001-24	openfda.package_ndc
ndc	package	42339-001-18	openfda.package_ndc
ndc	package	42339-001-04	openfda.package_ndc
ndc	package	42339-001-15	openfda.package_ndc
ndc	package	42339-001-19	openfda.package_ndc
ndc	package	42339-001-02	openfda.package_ndc
ndc	package	42339-001-10	openfda.package_ndc
ndc	package	42339-001-22	openfda.package_ndc
ndc	package	42339-001-27	openfda.package_ndc
ndc	package	42339-001-07	openfda.package_ndc
ndc	package	42339-001-28	openfda.package_ndc
ndc	package	42339-001-13	openfda.package_ndc
ndc	package	42339-001-25	openfda.package_ndc
ndc	package	42339-001-14	openfda.package_ndc
ndc	product	42339-001	openfda.product_ndc
ndc11	package	42339000105	derived:openfda.package_ndc
ndc11	package	42339000128	derived:openfda.package_ndc
ndc11	package	42339000113	derived:openfda.package_ndc
ndc11	package	42339000117	derived:openfda.package_ndc
ndc11	package	42339000119	derived:openfda.package_ndc
ndc11	package	42339000124	derived:openfda.package_ndc

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 with electrocautery procedures in eyes. Stop use and ask a doctor if irritation and redness develop,condition persists for more than 72 hours . keep out of reach of children In case of accidental ingestion, seek professional assistance or consult a PoisonControl Center immediately.

Reported adverse events (FAERS/openFDA)#

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