Scar Reducer Intensive Herbal and Nutrient

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: Scar Reducer Intensive Herbal and Nutrient
Generic name: ALLANTOIN
Manufacturer: Quantum, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 5197f1fa-aae5-406c-97d9-635b8c1a88a8
SPL ID: 40838898-6268-702c-e063-6394a90a8b3d
Version: 3
Effective date: 2025-10-06
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:46:07

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		Scar Reducer Intensive Herbal and Nutrient	openfda.brand_name
generic name		ALLANTOIN	openfda.generic_name
manufacturer name		Quantum, Inc	openfda.manufacturer_name
ndc	package	70084-710-01	openfda.package_ndc
ndc	product	70084-710	openfda.product_ndc
ndc11	package	70084071001	derived:openfda.package_ndc
rxcui		2001650	openfda.rxcui
spl id		40838898-6268-702c-e063-6394a90a8b3d	id
spl set id		5197f1fa-aae5-406c-97d9-635b8c1a88a8	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

Warnings For external use only When using this product do not get into eyes Stop use and ask doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days Do not use on deep or puncture wounds animal bites serious burns If pregnant or nursing, ask a health professional before use. Keep out of the 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.