Welly Polka First Aid Kit

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
Welly Polka First Aid Kit
Generic name
HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
Manufacturer
Dongguan Shenglian Tins Products Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
d7c4314c-c4c6-4adf-b384-3ac7a7108319
SPL ID
462a5bc7-4641-3c3d-e063-6394a90abb6c
Version
3
Effective date
2025-12-17
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:10:08

Warnings cross-check#

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Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only. Do not use ● in the eyes ● for treatment of diaper rash, consult a doctor. Stop use, ask a doctor ● if condition worsens, or if symptoms persist for more than 7 days or clears up and occurs again within a few days ● with use of any other hydrocortisone product Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

warnings

Warnings For external use only. Do not use ● In the eyes ● Over large areas of the body ● If you are allergic to any of the ingredients Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns. Stop use and ask a doctor if ● Condition persists or gets worse. ● You need to use longer than 1 week. ● A rash or other allergic reaction develops. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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