Amerfresh Medicated Body Powder

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
Amerfresh Medicated Body Powder
Generic name
MENTHOL AND ZINC OXIDE
Manufacturer
ONEST LIMITED
Product type
HUMAN OTC DRUG
SPL set ID
8bef552b-b110-4663-9347-f8dba96c8d53
SPL ID
50c0de03-0145-10bd-e063-6394a90ad3a4
Version
1
Effective date
2026-05-01
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:20
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

Warnings For external use only • Do not use • Broken skin • Deep or puncture wounds • Serious burns When using this product avoid contact with the eyes Keep away from face and mouth to avoid breathing powder. Stop use and ask a doctor : • If the condition worsens • Symptoms persist for more than 7 days or clear up and occur again within a few days. • Redness, irritation, swelling, or pain persists or increases. Keep out of 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.