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
1e01ecd8-8271-3947-e063-6294a90a69c6
SPL ID
29a7e1ed-c883-438b-e063-6394a90a0cb4
Version
2
Effective date
2024-12-19
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:49:21
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. Flammable, keep away from fire or flame. Do not use Do not use on broken skin Stop use Stop use if rash or irritation occurs. 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.