BODY DEODORIZERSPRAY

Manufacturer: Guangzhou Yanxi Biotechnology Co.. Ltd
Effective date: 2024-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:16:29

Label at a glance#

ProductBODY DEODORIZERSPRAY

Active ingredientALUMINUM CHLOROHYDRATE ANHYDROUS, POLYSORBATE 20

Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Spray for eliminating body odor

WARNINGS SECTION

keep out of children

INACTIVE INGREDIENT SECTION

Aqua

INDICATIONS & USAGE SECTION

For eliminating body odor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children

OTC - PURPOSE SECTION

Eliminates body odor and moisturizes skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

biaoqian

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84025-106-01	BODY DEODORIZERSPRAY	100 mL in 1 BOTTLE	SPRAY	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84025-106	BODY DEODORIZERSPRAY (BODY DEODORIZER SPRAY) SPRAY [GUANGZHOU YANXI BIOTECHNOLOGY CO.. LTD]	1	1 package rows	20240805_1e9c8386-0efa-8189-e063-6394a90af847.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

BODY DEODORIZERSPRAY
Body Deodorizer Spray
ALUMINUM CHLOROHYDRATE ANHYDROUS
POLYSORBATE 20
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84025-106	84025-106-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALUMINUM CHLOROHYDRATE ANHYDROUS	407PSC3OC7	ACTIB
POLYSORBATE 20	7T1F30V5YH	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1e9c8386-0efb-8189-e063-6394a90af847			1e9c8386-0efa-8189-e063-6394a90af847	2024-08-01	Warnings	Exact identifier spl id: 1e9c8386-0efb-8189-e063-6394a90af847 spl set id: 1e9c8386-0efa-8189-e063-6394a90af847

Reported adverse events (FAERS/openFDA)#

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