FDA.reportPublic FDA data

FDA label 0fc4ce37-bc88-4011-b41d-7fcce9efec50

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)

SPL set ID
6354d3e2-df70-4e61-bfaa-7a60bf6ac7eb
SPL ID
0fc4ce37-bc88-4011-b41d-7fcce9efec50
Version
4
Effective date
2017-01-27
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:16

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 Flammable. Keep away from heat and flame. When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice. Directions wet hands thoroughly with product and rub into skin until dry Children under 6 years of age should be supervised by an adult when using this product. Inactive Ingredients water (aqua), triethanolamine, carbomer, aloe barbadensis leaf juice, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E).

Reported adverse events (FAERS/openFDA)#

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