terrasil Bed Sore and Pressure 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 Bed Sore and Pressure Sore Relief
Generic name: ALLANTOIN
Manufacturer: Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Product type: HUMAN OTC DRUG
SPL set ID: d0e4a492-f833-4e92-bd4a-b0a07ce9a69e
SPL ID: 43e3a1df-9241-a075-e063-6294a90a4b88
Version: 4
Effective date: 2025-11-18
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 05:54:31

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 Bed Sore and Pressure 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	24909-035-45	openfda.package_ndc
ndc	package	24909-035-44	openfda.package_ndc
ndc	package	24909-035-85	openfda.package_ndc
ndc	product	24909-035	openfda.product_ndc
ndc11	package	24909003545	derived:openfda.package_ndc
ndc11	package	24909003544	derived:openfda.package_ndc
ndc11	package	24909003585	derived:openfda.package_ndc
rxcui		2668900	openfda.rxcui
spl id		43e3a1df-9241-a075-e063-6294a90a4b88	id
spl set id		d0e4a492-f833-4e92-bd4a-b0a07ce9a69e	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. 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.