Lume Soft 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
Lume Soft Powder
Generic name
ALUMINUM CHLOROHYDRATE
Manufacturer
Lume Deodorant, LLC.
Product type
HUMAN OTC DRUG
SPL set ID
47be0eea-097f-4030-e063-6294a90ad48c
SPL ID
4a6891f1-c41d-705e-e063-6294a90a53b7
Version
2
Effective date
2026-02-09
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:29:20
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. Flammable. Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Keep away fro face and mouth to avoid breathing in. Do not spray near flame or while smoking. Do not use on broken or irritated skin. Stop use if rash or irritation occurs Ask a doctor before use if you have kidney disease. Sunburn alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun expposure while using this product and for a week afterwards. Do not expose to heat or store at a temperature above 120F. Use only as directed. Intentional misuse by deliberaely concentrating and inhaling the contents can be harmful or fatal. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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