OTC Medication Information: Antiperspirant Dry 1.6 Oz Men Antiperspirant

ANTIPERSPIRANT DRY 1.6 OZ MEN ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray
Rejoice International Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient ………………………………………………………………… Purpose

Aluminum Chlorohydrate 23.3% ………………………………………….. Antiperspirant

Antiperspirant

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reduces underarm wetness

Warnings

For external use only.

Flammable. Do not use while smoking or near heat or flame or while smoking. Can cause serious injury or death.

• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. CONTENTS UNDER PRESSURE. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120 ^o F/50 ^o C or in enclosed places that could overheat.
• Do not use on broken skin.
• Ask a doctor before using, if you have kidney disease
• When using this product.
• Keep away from face and mouth to avoid breathing it
• avoid spraying in eyes
• USE ONLY AS DIRECTED. INTENTIONAL MISSUSE BY DELIBERATELY CONCENTRATING AND INHAILING THE CONTENTS CAN BE HARMFUL OR FATAL.
• Stop use if rash or irritation occurs

Directions

• For underarm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm and spray

Inactive Ingredients

Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Bentonite, Lauryl Phosphate

ANTIPERSPIRANT DRY 1.6 OZ MEN ANTIPERSPIRANT aluminum chlorohydrate aerosol, spray

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57337-109 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE 23.3 g in 100 g

Inactive Ingredients Ingredient Name Strength ALCOHOL BUTYLATED HYDROXYTOLUENE DISTEARDIMONIUM HECTORITE .ALPHA.-TOCOPHEROL ACETATE SUNFLOWER OIL BUTANE ISOPROPYL MYRISTATE ALUMINUM STARCH OCTENYLSUCCINATE DIMETHICONE PPG-14 BUTYL ETHER ALKYL (C12-15) BENZOATE PROPANE BENTONITE 1,1-DIFLUOROETHANE CYCLOMETHICONE 5

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:57337-109-01 45 g in 1 BOTTLE, SPRAY None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 01/13/2020

Labeler — Rejoice International Inc (078741245)

Establishment
Name	Address	ID/FEI	Operations
BLUE SEA AEROSOL & DAILY CARE CO., LTD.		544373091	manufacture (57337-109)

Revised: 05/2021 Rejoice International Inc