Mando - Mt. Fuji

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: Mando - Mt. Fuji
Generic name: ALUMINUM SESQUICHLOROHYDRATE
Manufacturer: Lume Deodorant, LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 351d20eb-3cf4-e28b-e063-6294a90a4cf0
SPL ID: 485ccd95-ccb7-eef0-e063-6294a90a2581
Version: 3
Effective date: 2026-01-14
Source export date: 2026-10-27
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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:59:41

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M019	openfda.application_number
brand name		Mando - Pro Sport	openfda.brand_name
brand name		Mando Deodorant plus Extra Strength Sweat Control - Pro Sport	openfda.brand_name
brand name		Mando Deodorant plus Extra Strength Sweat Control - Clover Woods	openfda.brand_name
brand name		Mando Deodorant plus Extra Strength Sweat Control - Cedar Grove	openfda.brand_name
brand name		Mando - Mt. Fuji	openfda.brand_name
generic name		ALUMINUM SESQUICHLOROHYDRATE	openfda.generic_name
manufacturer name		Lume Deodorant, LLC.	openfda.manufacturer_name
ndc	package	84520-009-01	openfda.package_ndc
ndc	package	84520-006-01	openfda.package_ndc
ndc	package	84520-007-01	openfda.package_ndc
ndc	package	84520-008-01	openfda.package_ndc
ndc	package	84520-005-01	openfda.package_ndc
ndc	package	84520-010-01	openfda.package_ndc
ndc	product	84520-010	openfda.product_ndc
ndc	product	84520-005	openfda.product_ndc
ndc	product	84520-009	openfda.product_ndc
ndc	product	84520-007	openfda.product_ndc
ndc	product	84520-006	openfda.product_ndc
ndc	product	84520-008	openfda.product_ndc
ndc11	package	84520000901	derived:openfda.package_ndc
ndc11	package	84520000601	derived:openfda.package_ndc
ndc11	package	84520000701	derived:openfda.package_ndc
ndc11	package	84520000501	derived:openfda.package_ndc
ndc11	package	84520000801	derived:openfda.package_ndc
ndc11	package	84520001001	derived:openfda.package_ndc
spl id		485ccd95-ccb7-eef0-e063-6294a90a2581	id
spl set id		351d20eb-3cf4-e28b-e063-6294a90a4cf0	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.