Desitin Maximum Strength Diaper Rash

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: Desitin Maximum Strength Diaper Rash
Generic name: ZINC OXIDE
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: af64fc2f-c027-4a68-b368-ee06744a2452
SPL ID: 26dd439f-d784-6c9b-e063-6394a90a3eff
Version: 8
Effective date: 2024-11-15
Source export date: 2026-10-30
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:26:45

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Desitin Maximum Strength Diaper Rash	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0061-4	openfda.package_ndc
ndc	package	69968-0061-5	openfda.package_ndc
ndc	package	69968-0061-1	openfda.package_ndc
ndc	package	69968-0061-3	openfda.package_ndc
ndc	package	69968-0061-9	openfda.package_ndc
ndc	package	69968-0061-7	openfda.package_ndc
ndc	package	69968-0061-2	openfda.package_ndc
ndc	product	69968-0061	openfda.product_ndc
ndc11	package	69968006109	derived:openfda.package_ndc
ndc11	package	69968006102	derived:openfda.package_ndc
ndc11	package	69968006105	derived:openfda.package_ndc
ndc11	package	69968006104	derived:openfda.package_ndc
ndc11	package	69968006107	derived:openfda.package_ndc
ndc11	package	69968006103	derived:openfda.package_ndc
ndc11	package	69968006101	derived:openfda.package_ndc
rxcui		1094560	openfda.rxcui
rxcui		1797059	openfda.rxcui
spl id		26dd439f-d784-6c9b-e063-6394a90a3eff	id
spl set id		af64fc2f-c027-4a68-b368-ee06744a2452	set_id
unii		SOI2LOH54Z	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 When using this product do not get into eyes Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days 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.