Kenaf wet wipe kids

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
Kenaf wet wipe kids
Generic name
ALLANTOIN
Manufacturer
MEDICELL BIO CO., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
86106dd8-b20b-15ee-e053-2991aa0aa7b2
SPL ID
384bba7f-997a-8686-e063-6294a90a0545
Version
3
Effective date
2025-06-24
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:38
Harmonized routes table
Harmonized routes
TOPICAL

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

1. For external use only. 1) Do not use over the wound and irritated skin with eczema or infections 2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help 2. Keep the cover closed tight after use 3. Do not put the left over contents back into the container to avoid deterioration 1) Avoid contact with eyes 2) Keep out of reach of children 3) Store in a cool and dry place, away from direct sun light

Reported adverse events (FAERS/openFDA)#

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