Dawn Ultra Antibacterial Hand Orange Scent

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: Dawn Ultra Antibacterial Hand Orange Scent
Generic name: CHLOROXYLENOL
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: b440e526-83c2-45b7-9c45-f95151216000
SPL ID: 4e66f27a-c14a-2596-e063-6394a90a7853
Version: 16
Effective date: 2026-04-01
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:05

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 · 52 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Dawn Ultra Antibacterial Hand Orange Scent	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	37000-617-82	openfda.package_ndc
ndc	package	37000-617-21	openfda.package_ndc
ndc	package	37000-617-65	openfda.package_ndc
ndc	package	37000-617-10	openfda.package_ndc
ndc	package	37000-617-91	openfda.package_ndc
ndc	package	37000-617-16	openfda.package_ndc
ndc	package	37000-617-11	openfda.package_ndc
ndc	package	37000-617-12	openfda.package_ndc
ndc	package	37000-617-19	openfda.package_ndc
ndc	package	37000-617-57	openfda.package_ndc
ndc	package	37000-617-26	openfda.package_ndc
ndc	package	37000-617-40	openfda.package_ndc
ndc	package	37000-617-53	openfda.package_ndc
ndc	package	37000-617-47	openfda.package_ndc
ndc	package	37000-617-70	openfda.package_ndc
ndc	package	37000-617-22	openfda.package_ndc
ndc	package	37000-617-63	openfda.package_ndc
ndc	package	37000-617-20	openfda.package_ndc
ndc	package	37000-617-23	openfda.package_ndc
ndc	package	37000-617-59	openfda.package_ndc
ndc	package	37000-617-38	openfda.package_ndc
ndc	package	37000-617-54	openfda.package_ndc
ndc	product	37000-617	openfda.product_ndc
ndc11	package	37000061711	derived:openfda.package_ndc
ndc11	package	37000061726	derived:openfda.package_ndc
ndc11	package	37000061722	derived:openfda.package_ndc
ndc11	package	37000061712	derived:openfda.package_ndc
ndc11	package	37000061757	derived:openfda.package_ndc
ndc11	package	37000061710	derived:openfda.package_ndc
ndc11	package	37000061770	derived:openfda.package_ndc
ndc11	package	37000061765	derived:openfda.package_ndc
ndc11	package	37000061740	derived:openfda.package_ndc
ndc11	package	37000061723	derived:openfda.package_ndc
ndc11	package	37000061721	derived:openfda.package_ndc
ndc11	package	37000061753	derived:openfda.package_ndc
ndc11	package	37000061763	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 Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Reported adverse events (FAERS/openFDA)#

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