Moisture Barrier

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: Moisture Barrier
Generic name: MENTHOL 0.44%, ZINC OXIDE 20.6%
Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
SPL set ID: 258f3392-0f42-21e8-e063-6294a90ae9ad
SPL ID: 5734b3f2-f7b4-4a9f-e063-6394a90ac8d1
Version: 3
Effective date: 2026-07-22
Source export date: 2026-11-06
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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:04:06

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Moisture Barrier	openfda.brand_name
generic name		MENTHOL 0.44%, ZINC OXIDE 20.6%	openfda.generic_name
manufacturer name		Walgreen Company	openfda.manufacturer_name
ndc	package	0363-6254-07	openfda.package_ndc
ndc	product	0363-6254	openfda.product_ndc
ndc11	package	00363625407	derived:openfda.package_ndc
rxcui		2123045	openfda.rxcui
spl id		5734b3f2-f7b4-4a9f-e063-6394a90ac8d1	id
spl set id		258f3392-0f42-21e8-e063-6294a90ae9ad	set_id
unii		L7T10EIP3A	openfda.unii
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 exceed the recommended daily dosage unless directed by a doctor Do not put this product into the rectum by using fingers or any mechanical device or applicator Stop use and ask a doctor if condition worsens or does not improve within 7 days bleeding occurs the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase If pregnant or breast feeding, ask a health professional before use. 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.