Redicare Burn Gel

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
Redicare Burn Gel
Generic name
REDICARE BURN GEL
Manufacturer
Redicare LLC
Product type
HUMAN OTC DRUG
SPL set ID
947ac362-acfb-3508-e053-2a95a90a2873
SPL ID
2f9cfcad-603b-4de7-e063-6294a90a6172
Version
2
Effective date
2025-03-05
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:53:34
Harmonized routes table
Harmonized routes
TOPICAL

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 In large quantities, particularly over raw or blistered areas near eyes, if this happens rinse thoroughly with water. Stop use and ask doctor if condition worsens or persists for more than 7 days or clears up and occurs again within a few days Keep out of 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.