SURE ORIGINAL SOLID UNSCENTED- aluminum zirconium trichlorohydrex gly stick

Sure Original Solid Unscented by

Drug Labeling and Warnings

Sure Original Solid Unscented by is a Otc medication manufactured, distributed, or labeled by Sodalis USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Aluminum Zirconium trichlorohydrex GLY 16% 

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only.

Stop use if 

rash or irritation occurs.

Do not use 

on broken skin.

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center right away.

Ask a doctor before use if you have

kidney disease.

Directions

apply to underarms only.

Inactive ingredients:

Cyclopentasiloxane, Stearyl Alcohol, Talc, Dimethicone, Hydrogenated Castor Oil, Dipropylene Glycol, Silica, Polyethylene, Behenyl Alcohol, Pentadecalactone

Questions?

1-800-575-7960

Label

INGREDIENTS AND APPEARANCE

SURE ORIGINAL SOLID UNSCENTED 
aluminum zirconium trichlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81277-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	19 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TALC (UNII: 7SEV7J4R1U)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
DOCOSANOL (UNII: 9G1OE216XY)
PENTADECALACTONE (UNII: OK17S3S98K)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81277-005-01	76 g in 1 CONTAINER; Type 0: Not a Combination Product	12/22/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	12/22/2009

Labeler - Sodalis USA LLC (119375257)