Betadine 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: Betadine Surgical Scrub
Generic name: POVIDONE-IODINE
Manufacturer: Atlantis Consumer Healthcare, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1ad39e11-ea1e-44a4-8224-93f8135436c2
SPL ID: 26bf0dc4-726a-4f00-a3f8-1672431c6899
Version: 11
Effective date: 2025-01-06
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:26:08

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Betadine Surgical Scrub	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Atlantis Consumer Healthcare, Inc.	openfda.manufacturer_name
ndc	package	67618-151-04	openfda.package_ndc
ndc	package	67618-151-32	openfda.package_ndc
ndc	package	67618-151-17	openfda.package_ndc
ndc	package	67618-151-01	openfda.package_ndc
ndc	package	67618-151-16	openfda.package_ndc
ndc	product	67618-151	openfda.product_ndc
ndc11	package	67618015101	derived:openfda.package_ndc
ndc11	package	67618015116	derived:openfda.package_ndc
ndc11	package	67618015132	derived:openfda.package_ndc
ndc11	package	67618015117	derived:openfda.package_ndc
ndc11	package	67618015104	derived:openfda.package_ndc
rxcui		1149658	openfda.rxcui
rxcui		211747	openfda.rxcui
spl id		26bf0dc4-726a-4f00-a3f8-1672431c6899	id
spl set id		1ad39e11-ea1e-44a4-8224-93f8135436c2	set_id
unii		85H0HZU99M	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 Do not use this product in the eyes When using this product prolonged exposure to wet solution may cause irritation or, rarely, severe skin reactions Stop use and ask a doctor if irritation and redness develop in rare instances of local irritation or sensitivity 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.