Chamosyn

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: Chamosyn
Generic name: BARRIER CREAM
Manufacturer: Links Medical Products
Product type: HUMAN OTC DRUG
SPL set ID: f9dfb2d7-4684-4525-994e-1e0ff90413d9
SPL ID: 34a97f44-835c-ebb7-e063-6294a90a5b67
Version: 8
Effective date: 2025-05-08
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:28

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Chamosyn	openfda.brand_name
brand name		Chamosyn Paraben Free	openfda.brand_name
generic name		BARRIER CREAM	openfda.generic_name
manufacturer name		Links Medical Products	openfda.manufacturer_name
ndc	package	51028-001-01	openfda.package_ndc
ndc	package	51028-003-01	openfda.package_ndc
ndc	package	51028-002-01	openfda.package_ndc
ndc	package	51028-001-00	openfda.package_ndc
ndc	package	51028-003-00	openfda.package_ndc
ndc	product	51028-001	openfda.product_ndc
ndc	product	51028-002	openfda.product_ndc
ndc	product	51028-003	openfda.product_ndc
ndc11	package	51028000100	derived:openfda.package_ndc
ndc11	package	51028000301	derived:openfda.package_ndc
ndc11	package	51028000101	derived:openfda.package_ndc
ndc11	package	51028000201	derived:openfda.package_ndc
ndc11	package	51028000300	derived:openfda.package_ndc
rxcui		2730301	openfda.rxcui
rxcui		1998442	openfda.rxcui
rxcui		884804	openfda.rxcui
spl id		34a97f44-835c-ebb7-e063-6294a90a5b67	id
spl set id		f9dfb2d7-4684-4525-994e-1e0ff90413d9	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 get into eyes Stop use and ask a doctor if condition worsens symptoms do not improve within 7 days or clear up and occur again within a few days. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any medical device or applicator. Certain persons can develop allergic reactions to this product. If symptoms do not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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