terrasil Skin Repair

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: terrasil Skin Repair
Generic name: ALLANTOIN
Manufacturer: Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Product type: HUMAN OTC DRUG
SPL set ID: 92a23c7f-6b89-49cb-93e2-49ab7a85c86d
SPL ID: 39b20e15-cdd0-2779-e063-6294a90afdc5
Version: 4
Effective date: 2025-07-11
Source export date: 2026-10-27
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/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:57:29

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		terrasil Skin Repair	openfda.brand_name
generic name		ALLANTOIN	openfda.generic_name
manufacturer name		Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	openfda.manufacturer_name
ndc	package	24909-032-14	openfda.package_ndc
ndc	package	24909-032-21	openfda.package_ndc
ndc	package	24909-032-20	openfda.package_ndc
ndc	package	24909-032-50	openfda.package_ndc
ndc	package	24909-032-28	openfda.package_ndc
ndc	product	24909-032	openfda.product_ndc
ndc11	package	24909003228	derived:openfda.package_ndc
ndc11	package	24909003221	derived:openfda.package_ndc
ndc11	package	24909003214	derived:openfda.package_ndc
ndc11	package	24909003250	derived:openfda.package_ndc
ndc11	package	24909003220	derived:openfda.package_ndc
rxcui		1044541	openfda.rxcui
spl id		39b20e15-cdd0-2779-e063-6294a90afdc5	id
spl set id		92a23c7f-6b89-49cb-93e2-49ab7a85c86d	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 a 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 or serious burns. K eep out of reach of children. If swallowed, call Poison Control or seek medical help. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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