DawnMist Antiperspirant

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
DawnMist Antiperspirant
Generic name
ALUMINUM CHLOROHYDRATE
Manufacturer
Dukal LLC
Product type
HUMAN OTC DRUG
SPL set ID
1e17daf8-075e-e331-e063-6294a90ad11c
SPL ID
29a89490-b70d-4a41-e063-6294a90a90ea
Version
2
Effective date
2024-12-19
Source export date
2026-10-30
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/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:33:59
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 Do not use on broken skin Ask a doctor before use Ask a doctor before use if you have kidney disease. Keep out of reach of children Keep out of reach of children. If accidently swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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