OLD SPICE SWEAT DEFENSE KNOCKOUT DRY ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray

Old Spice Sweat Defense Knockout Dry Antiperspirant by

Drug Labeling and Warnings

Old Spice Sweat Defense Knockout Dry Antiperspirant by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Aluminum chlorohydrate 24.5% (anhydrous)

Purpose

Antiperspirant

Use

• reduces underarm wetness

Warnings

For external use only.

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

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

When using this product

keep away from face and mouth to avoid breathing it

avoid spraying in eyes

use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

SAFE HANDLING WARNING

Flammable

do not spray near flame or while smoking

contents under pressure
do not crush, puncture or incinerate

do not expose to heat or store at temperature above 120ºF

Directions

• apply to underarms only

Inactive ingredients

Butane, hydrofluorocarbon 152A, dimethicone, C12-15 alkyl benzoate, isopropyl myristate, PPG-14 butyl ether, fragrance, disteardimonium hectorite, mineral oil, propylene carbonate, corn starch/maltodextrin crosspolymer, dimethiconol, argania spinosa kernel oil

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

Questions or comments?

1-800-677-7582

PRINCIPAL DISPLAY PANEL - 122 g Can

Old Spice ®

SWEAT DEFENSE

KNOCKOUT

DRY SPRAY

SIZE XL

48 HR LASTING FRESHNESS

ALUMINUM CHLOROHYDRATE

ANTIPERSPIRANT

NET WT. 4.3 OZ (122 g)

INGREDIENTS AND APPEARANCE

OLD SPICE SWEAT DEFENSE KNOCKOUT DRY ANTIPERSPIRANT 
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-682
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	24.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
BUTANE (UNII: 6LV4FOR43R)
HYDROFLUOROCARBON 152A (UNII: 0B1U8K2ME0)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DIMETHICONE (UNII: 92RU3N3Y1O)
MINERAL OIL (UNII: T5L8T28FGP)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ARGAN OIL (UNII: 4V59G5UW9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-682-12	122 g in 1 CAN; Type 0: Not a Combination Product	01/01/2022	09/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/01/2022	09/01/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)