FDA label abdaec0e-aac3-4b79-a9be-8e1efd491cc6

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
5ed388ed-ed1b-4f83-bc20-1f737233c154
SPL ID
abdaec0e-aac3-4b79-a9be-8e1efd491cc6
Version
1
Effective date
2013-06-27
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 06:12:41

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 flame or high heat. When using this product Avoid contact with eyes. If contact occurs flush eyes with water. Avoid contact with broken skin Directions Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommeded for infants Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf juice, Ultra marines (CI 77007) May Contain: Red 4 (CI 14700), Yellow 5 (CI 19140), Blue 1 (CI 42090), Red 33 (CI 17200).

Reported adverse events (FAERS/openFDA)#

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