LESONEL FEMININE FOAMING WASH

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)

Brand name
LESONEL FEMININE FOAMING WASH
Generic name
ALLANTOIN
Manufacturer
ACE PHARMACEUTICAL CO.,LTD.
Product type
HUMAN OTC DRUG
SPL set ID
3033b1b3-21b7-9b5b-e063-6294a90a54c5
SPL ID
3033bf9e-0e48-de43-e063-6394a90ab14d
Version
1
Effective date
2025-03-13
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:18:21
Harmonized routes table
Harmonized routes
VAGINAL

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. If you notice any unusual symptoms or side effects such as redness, swelling, or itching in the area where the cosmetic product was applied, particularly after direct sunlight exposure during or after use, seek advice from a specialist or health care professional 2. Do not apply on broken or irritated skin. 3. Precautions for Safe Handling: a. Keep out of reach of children b. Store in a cool, dry place and away from direct sunlight. 4. Use exclusively on the external genital area; avoid internal vaginal application 5. Follow the recommended usage instructions on the product packaging 6. Avoid application on children under 3 years old 7. Avoid use during pregnancy and refrain from application around the external genital area immediately before childbirthPrecautions for Safe Handling: a. Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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