Burn Ease 3.5g

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: Burn Ease 3.5g
Generic name: BURN EASE 3.5G
Manufacturer: Front Line Safety
Product type: HUMAN OTC DRUG
SPL set ID: 0f8e6842-c889-d5d3-e063-6394a90af880
SPL ID: 46015808-761f-ab92-e063-6294a90a5ab0
Version: 3
Effective date: 2025-12-15
Source export date: 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:57:12

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		M017	openfda.application_number
brand name		Burn Ease 3.5g	openfda.brand_name
generic name		BURN EASE 3.5G	openfda.generic_name
manufacturer name		Front Line Safety	openfda.manufacturer_name
ndc	package	58228-6283-1	openfda.package_ndc
ndc	product	58228-6283	openfda.product_ndc
ndc11	package	58228628301	derived:openfda.package_ndc
rxcui		1011852	openfda.rxcui
spl id		46015808-761f-ab92-e063-6294a90a5ab0	id
spl set id		0f8e6842-c889-d5d3-e063-6394a90af880	set_id
unii		V13007Z41A	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 Do not use • On wounds or damaged skin • In large quantities, particulary over raw surfaces or blistered areas When using this product • Avoid contact with the eyes • Do not bandage tightly Stop use and ask a doctor if • Condition worsens • Symptoms persist for more than 7 days • Symptoms clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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