OLD SPICE OASIS WITH VANILLA NOTES DRY- aluminum sesquichlorohydrate aerosol, spray

Old Spice Oasis with Vanilla Notes Dry by

Drug Labeling and Warnings

Old Spice Oasis with Vanilla Notes Dry 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 24.5.0% (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

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 ®

OASIS

with VANILLA NOTES

ANTIPERSPIRANT

DRY SPRAY

24/7 LASTING

SWEAT DEFENSE

ALUMINUM CHLOROHYDRATE

ANTIPERSPIRANT

NET WT. 4.3 OZ (122 g)

INGREDIENTS AND APPEARANCE

OLD SPICE OASIS WITH VANILLA NOTES DRY 
aluminum sesquichlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE ANHYDROUS (UNII: 407PSC3OC7) (ALUMINUM CHLOROHYDRATE ANHYDROUS - UNII:407PSC3OC7)	ALUMINUM CHLOROHYDRATE ANHYDROUS	24.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
BUTANE (UNII: 6LV4FOR43R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-036-12	122 g in 1 CAN; Type 0: Not a Combination Product	02/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	02/01/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)