DOCOSANOL

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: DOCOSANOL
Generic name: DOCOSANOL
Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
SPL set ID: 9f361f24-a0a1-4e43-a158-8c830c9adca7
SPL ID: 6dcfa761-32bb-4b0e-b0c0-2bd44cfe99d9
Version: 3
Effective date: 2026-06-10
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:38:54

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	217090	derived:openfda.application_number
application number		ANDA217090	openfda.application_number
brand name		DOCOSANOL	openfda.brand_name
generic name		DOCOSANOL	openfda.generic_name
manufacturer name		Aurohealth LLC	openfda.manufacturer_name
ndc	package	58602-019-12	openfda.package_ndc
ndc	package	58602-019-17	openfda.package_ndc
ndc	package	58602-019-11	openfda.package_ndc
ndc	package	58602-019-24	openfda.package_ndc
ndc	package	58602-019-09	openfda.package_ndc
ndc	package	58602-019-08	openfda.package_ndc
ndc	package	58602-019-13	openfda.package_ndc
ndc	package	58602-019-15	openfda.package_ndc
ndc	package	58602-019-16	openfda.package_ndc
ndc	product	58602-019	openfda.product_ndc
ndc11	package	58602001917	derived:openfda.package_ndc
ndc11	package	58602001911	derived:openfda.package_ndc
ndc11	package	58602001912	derived:openfda.package_ndc
ndc11	package	58602001924	derived:openfda.package_ndc
ndc11	package	58602001915	derived:openfda.package_ndc
ndc11	package	58602001909	derived:openfda.package_ndc
ndc11	package	58602001913	derived:openfda.package_ndc
ndc11	package	58602001908	derived:openfda.package_ndc
ndc11	package	58602001916	derived:openfda.package_ndc
rxcui		797534	openfda.rxcui
spl id		6dcfa761-32bb-4b0e-b0c0-2bd44cfe99d9	id
spl set id		9f361f24-a0a1-4e43-a158-8c830c9adca7	set_id
unii		9G1OE216XY	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 Allergy alert: This product may cause a severe allergic reaction. Symptoms may include: • hives • facial swelling • wheezing/difficulty breathing • shock • rash If an allergic reaction occurs, stop use and seek medical help right away. For external use only

Reported adverse events (FAERS/openFDA)#

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