PURELL Waterless Surgical Scrub

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: PURELL Waterless Surgical Scrub
Generic name: ALCOHOL
Manufacturer: GOJO Industries, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e3ed5e0c-1e21-47eb-a999-9c8aa5083dff
SPL ID: 29676456-b1d3-defb-e063-6394a90a0091
Version: 4
Effective date: 2024-12-16
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:52

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		PURELL Waterless Surgical Scrub	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		GOJO Industries, Inc.	openfda.manufacturer_name
ndc	package	21749-992-33	openfda.package_ndc
ndc	package	21749-992-02	openfda.package_ndc
ndc	package	21749-992-89	openfda.package_ndc
ndc	product	21749-992	openfda.product_ndc
ndc11	package	21749099202	derived:openfda.package_ndc
ndc11	package	21749099289	derived:openfda.package_ndc
ndc11	package	21749099233	derived:openfda.package_ndc
rxcui		582753	openfda.rxcui
spl id		29676456-b1d3-defb-e063-6394a90a0091	id
spl set id		e3ed5e0c-1e21-47eb-a999-9c8aa5083dff	set_id
unii		3K9958V90M	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 Flammable. Keep away from fire or flame. For external use only Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase the risk of sunburn. Take steps to limit sun exposure while using this product and for one week following use. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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