FDA label 4ff4ab7a-21d5-ed67-e063-6294a90ae31e

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
c554345f-9805-4b75-b4b7-8bdd78dbbbb7
SPL ID
4ff4ab7a-21d5-ed67-e063-6294a90ae31e
Version
2
Effective date
2026-04-21
Source export date
2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:25:54

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 as directed. Allergy alert get medical help right away if you develop hives, swelling of eyes and mouth, blistering, or difficulty breathing. Ask a doctor before use if you have severe acne. When using this product skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one product at a time • avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if • you develop severe irritation, burning or itching of the skin. • improvement is not apparent within 6-8 weeks. Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away. It is recommended that prior to exposure to the sun, users cover areas where AHAs have been applied with sunscreen.

Reported adverse events (FAERS/openFDA)#

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