MAXX PRO DRY ANTIPERSPIRANT AND DEODORANT COOL BLAST

Manufacturer: New Pride Corp
Effective date: 2023-04-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 21:33:17

Label at a glance#

ProductMAXX PRO DRY ANTIPERSPIRANT AND DEODORANT COOL BLAST

Active ingredientALUMINUM CHLOROHYDRATE

Label structure10 sections

Indications and uses

Reduce underarm wetness & perspiration.

Dosage and administration

Apply evenly to underarms only.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrates 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses:

INDICATIONS & USAGE SECTION

Reduce underarm wetness & perspiration.

Warnings:

WARNINGS SECTION

For external use only

Do not use:

OTC - DO NOT USE SECTION

On broken or irritated skin.

Stop use & ask a doctor:

OTC - STOP USE SECTION

if irritation or rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

If swallowed, seek medical help or contact a Posion Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply evenly to underarms only.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Mineral Oil, Ceresin, Beeswax, Corn Starch, Fragrance, Cyclopentasiloxane.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

MAXX PRO DRY ANTIPERSPIRANT AND DEODORANT COOL BLAST
aluminum chlorohydrate
MINERAL OIL
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)
PEG-8 BEESWAX
STARCH, CORN
CERESIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58037-201	58037-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MINERAL OIL	T5L8T28FGP	IACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)	UF7620L1W6	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
PEG-8 BEESWAX	3C1QUF1TIR	IACT
STARCH, CORN	O8232NY3SJ	IACT
CERESIN	Q1LS2UJO3A	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
f8bbc7bc-6d4c-e06f-e053-6394a90a3b16			f8bbc7bc-6d4b-e06f-e053-6394a90a3b16	2023-04-01	Warnings	Exact identifier spl id: f8bbc7bc-6d4c-e06f-e053-6394a90a3b16 spl set id: f8bbc7bc-6d4b-e06f-e053-6394a90a3b16

Reported adverse events (FAERS/openFDA)#

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