FDA label 48563c09-80f1-ed09-e063-6394a90a402c

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
3dcc4075-7ce7-d6a3-e063-6394a90a8f66
SPL ID
48563c09-80f1-ed09-e063-6394a90a402c
Version
2
Effective date
2026-01-14
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:53

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 1. Please read the instructions carefully beforeuse. Use the product within its shelf life. Do not use if the packaging is damaged or if it has expired. 2. This product should be used up in one go after opening the single-use packaging. 3. Use after menstruation ends. Lactating women and women without sexual history should use under the guidance of a doctor. 4. Wash your hands thoroughly before use. If you experience any burning sensation, redness, or swelling during use, discontinue use, cleanse the affected area promptly, and consult a doctor if necessary. 5. This product is for external use only. Do not take orally. Keep it out of reach of children. 6. It is recommended to use this product alone; if combined medication is necessary, please consult a doctor.

Reported adverse events (FAERS/openFDA)#

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