terrasil Diabetics Ulcer and Sore Relief

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 Diabetics Ulcer and Sore Relief
Generic name: ALLANTOIN
Manufacturer: Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Product type: HUMAN OTC DRUG
SPL set ID: fd6bf169-f1e2-48d4-b98d-8f3c39981a89
SPL ID: 35d2c97c-7eeb-d790-e063-6294a90af0ea
Version: 3
Effective date: 2025-05-23
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:24

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		terrasil Diabetics Ulcer and Sore Relief	openfda.brand_name
generic name		ALLANTOIN	openfda.generic_name
manufacturer name		Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	openfda.manufacturer_name
ndc	package	24909-034-44	openfda.package_ndc
ndc	package	24909-034-28	openfda.package_ndc
ndc	package	24909-034-14	openfda.package_ndc
ndc	product	24909-034	openfda.product_ndc
ndc11	package	24909003444	derived:openfda.package_ndc
ndc11	package	24909003414	derived:openfda.package_ndc
ndc11	package	24909003428	derived:openfda.package_ndc
rxcui		2668900	openfda.rxcui
spl id		35d2c97c-7eeb-d790-e063-6294a90af0ea	id
spl set id		fd6bf169-f1e2-48d4-b98d-8f3c39981a89	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. Consult a doctor before using on deep or puncture wounds, animal bites or serious burns. Keep out of reach of children. If swallowed, call Poison Control or seek medical help.

Reported adverse events (FAERS/openFDA)#

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