PERSONAL CARE QUICK DRY ANTIPERSPIRANT- aluminum chlorohydrate 20.2% spray

Personal CARE by

Drug Labeling and Warnings

Personal CARE by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum Chlorohydrate 20.2%

PURPOSE

Purpose  Antiperspirant

INDICATIONS & USAGE

Use reduces underarm wetness

Warnings

Flammable. Do not use near heat, 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 heal or store at temperature
above 120°F/SO"C or in enclosed places that
could overheat ■ do not use on broken skin.

STOP USE

Stop use if rash or irritation occurs

ASK DOCTOR

ask a doctor before using if you have kidney disease

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OTHER SAFETY INFORMATION

Use only as directed. Intentional misuse
by deliberately concentrating and Inhaling
the contents can be harmful or fatal.
Help stop inhalation abuse.
For information visit www.inhalant.org

DOSAGE & ADMINISTRATION

Directions ■ hold can 6 inches away from
the underarm ■ apply to underarms only

INACTIVE INGREDIENT

Inactive Ingredients
butane, hydrofluorocarbon 152A, cyclopentasiloxane, alcohol denat.,
PPG-14 butyl ether, isobutane, propane, disteardimonium, hectorlte, C12-15 alkyl
benzoate, helianthus annuus (sunflower) seed oil, dimethiconol,
propylene carbonate, octyIdodecanol,
fragrance, tocopheryl acetate, BHT

Package Label

INGREDIENTS AND APPEARANCE

PERSONAL CARE  QUICK DRY ANTIPERSPIRANT
aluminum chlorohydrate 20.2% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-905
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTANE (UNII: 6LV4FOR43R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ALCOHOL (UNII: 3K9958V90M)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
ISOBUTANE (UNII: BXR49TP611)
PROPANE (UNII: T75W9911L6)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SUNFLOWER OIL (UNII: 3W1JG795YI)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
OCTYLDODECANOL (UNII: 461N1O614Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-905-34	34 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/01/2019
2	NDC: 20276-905-45	45 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	02/01/2019

Labeler - Delta Brands Inc (102672008)