Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, 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 Whole Body Deodorant Plus Sweat Control Smooth Solid, Soft Powder
Generic name: ALUMINUM SESQUICHLOROHYDRATE
Manufacturer: Lume Deodorant, LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 1cebcddc-fa0f-8b73-e063-6394a90ab95e
SPL ID: 485c8837-f469-6d93-e063-6394a90a1dab
Version: 3
Effective date: 2026-01-14
Source export date: 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:59:12

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 31 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M019	openfda.application_number
brand name		Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Soft Powder	openfda.brand_name
brand name		Lume Deodorant with Clinical Strength Sweat Control, Vanilla Bliss	openfda.brand_name
brand name		Lume Deodorant with Clinical Strength Sweat Control, Soft Powder	openfda.brand_name
brand name		Lume Deodorant with Clinical Strength Sweat Control, Fresh Spring	openfda.brand_name
generic name		ALUMINUM SESQUICHLOROHYDRATE	openfda.generic_name
manufacturer name		Lume Deodorant, LLC.	openfda.manufacturer_name
ndc	package	84520-001-01	openfda.package_ndc
ndc	package	84520-003-01	openfda.package_ndc
ndc	package	84520-002-01	openfda.package_ndc
ndc	package	84520-034-01	openfda.package_ndc
ndc	package	84520-004-01	openfda.package_ndc
ndc	package	84520-014-01	openfda.package_ndc
ndc	package	84520-024-01	openfda.package_ndc
ndc	product	84520-004	openfda.product_ndc
ndc	product	84520-024	openfda.product_ndc
ndc	product	84520-002	openfda.product_ndc
ndc	product	84520-014	openfda.product_ndc
ndc	product	84520-034	openfda.product_ndc
ndc	product	84520-001	openfda.product_ndc
ndc	product	84520-003	openfda.product_ndc
ndc11	package	84520000401	derived:openfda.package_ndc
ndc11	package	84520000201	derived:openfda.package_ndc
ndc11	package	84520000101	derived:openfda.package_ndc
ndc11	package	84520000301	derived:openfda.package_ndc
ndc11	package	84520001401	derived:openfda.package_ndc
ndc11	package	84520003401	derived:openfda.package_ndc
ndc11	package	84520002401	derived:openfda.package_ndc
spl id		485c8837-f469-6d93-e063-6394a90a1dab	id
spl set id		1cebcddc-fa0f-8b73-e063-6394a90ab95e	set_id
unii		UCN889409V	openfda.unii

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 on broken or irritated skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs 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 exposure while using this product for a week afterwards.

Reported adverse events (FAERS/openFDA)#

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