ANTIPERSPIRANT DRY 1.6 OZ LADY ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray

Antiperspirant Dry 1.6 oz Lady by

Drug Labeling and Warnings

Antiperspirant Dry 1.6 oz Lady by is a Otc medication manufactured, distributed, or labeled by Rejoice International Inc., BLUE SEA AEROSOL & DAILY CARE CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient ........................................................................... Purpose

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

PURPOSE

Antiperspirant

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Reduces underarm wetness

WARNINGS

Warnings

For external use only.

Flammable.

Do not spray near flame or while smoking.
Contents under pressure
Do not crush, puncture or incinerate container.
Do not expose to heat or store at temperatures above 120oF
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 directed. Intentional missuse by deliberately concentrating and inhaling the contents can be harmful or fatal
Stop use if rash or irritation develops.

DOSAGE & ADMINISTRATION

Directions

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

INACTIVE INGREDIENT

Inactive Ingredients

Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Ethyl 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, Silica

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIPERSPIRANT DRY 1.6 OZ LADY  ANTIPERSPIRANT
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57337-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	23.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ISOBUTANE (UNII: BXR49TP611)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
SUNFLOWER OIL (UNII: 3W1JG795YI)
PROPANE (UNII: T75W9911L6)
LAURYL PHOSPHATE (UNII: 0K08L8GE2H)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57337-108-01	45 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/13/2020

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	Business Operations
BLUE SEA AEROSOL & DAILY CARE CO., LTD.		544373091	manufacture(57337-108)