DCH Scar

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: DCH Scar
Generic name: ALLANTOIN 0.5%
Manufacturer: Derma Care Research Labs, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 00edbc64-9d32-5751-e063-6294a90a400b
SPL ID: 29a4e82a-2134-3542-e063-6394a90a96a5
Version: 2
Effective date: 2024-12-19
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:13:08

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		DCH Scar	openfda.brand_name
generic name		ALLANTOIN 0.5%	openfda.generic_name
manufacturer name		Derma Care Research Labs, LLC	openfda.manufacturer_name
ndc	package	72839-097-01	openfda.package_ndc
ndc	product	72839-097	openfda.product_ndc
ndc11	package	72839009701	derived:openfda.package_ndc
rxcui		1442087	openfda.rxcui
spl id		29a4e82a-2134-3542-e063-6394a90a96a5	id
spl set id		00edbc64-9d32-5751-e063-6294a90a400b	set_id
unii		344S277G0Z	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

For external use only . When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. Do not use on deep or puncture wounds, animal bites, and serious burns.

Reported adverse events (FAERS/openFDA)#

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