FDA label 6f4008b5-0dde-4ebd-a8ab-c3c2641bc3c0

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
156d0a16-c18f-4d08-ac18-15c68bd2e6b5
SPL ID
6f4008b5-0dde-4ebd-a8ab-c3c2641bc3c0
Version
2
Effective date
2017-08-16
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:50

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 Warnings: 1. Stop use and ask doctor if any of the following symptoms occur. 1) Rash, swelling, itchiness, or irritation develops and lasts. 2) Rash, swelling, itchiness, or irritation on applied areas due to contact with direct sunlight. 2. Do not apply on wounds, areas inflicted with eczema, or dermatitis. 3. Guidelines for preservation/handling 1) Enclose lid/cap after use. 2) Keep out of reach of infants/young children. 3) Keep out of direct sunlight, and preserve in room temperature. 4) Scooping spilled materials back into the container may cause contamination. 4. Upon first use, make sure to apply a small dab, initially, in order to check for adverse reactions. 5. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Not to be swallowed If swallowed. 6. Do not swallow. If swallowed, get medical help or contact a poison control center right away. 7. Conditions for Preservation: 50~86 ℉. 8. SPF & UVA level has been indicated strictly by the "International SPF Test Method" and "KFDA (Korea Food and Drug Administration)". 7. For external use only

Reported adverse events (FAERS/openFDA)#

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