DiaperDerm 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: DiaperDerm Diaper Rash
Generic name: ZINC OXIDE
Manufacturer: Diaperderm Inc
Product type: HUMAN OTC DRUG
SPL set ID: 4e1fce3e-c2b7-42da-9953-1dbb13e2467c
SPL ID: 09762412-1b73-516e-e063-6294a90a6753
Version: 3
Effective date: 2023-11-06
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:07:15

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		DiaperDerm Diaper Rash	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Diaperderm Inc	openfda.manufacturer_name
ndc	package	80651-093-00	openfda.package_ndc
ndc	product	80651-093	openfda.product_ndc
ndc11	package	80651009300	derived:openfda.package_ndc
rxcui		1191136	openfda.rxcui
spl id		09762412-1b73-516e-e063-6294a90a6753	id
spl set id		4e1fce3e-c2b7-42da-9953-1dbb13e2467c	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, avoid contact with eyes. Stop use and ask a doctor if condition worsens or symptoms last more than 7 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.