TUSSY ANTIPERSPIRANT AND DEODORANT ORIGINAL FRESH SPICE- aluminum chlorohydrate liquid

Tussy Antiperspirant and Deodorant Original Fresh Spice by

Drug Labeling and Warnings

Tussy Antiperspirant and Deodorant Original Fresh Spice by is a Otc medication manufactured, distributed, or labeled by KCM Brands LLC, Suite K Value Added Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients                                     Purpose

Aluminum Chlorohydrate 19%                Antiperspirant

PURPOSE

Use reduces underarm perspiration

Use

reduce underarm perspiration

WARNINGS

Warnings For external use only

ASK DOCTOR

Ask a doctor before use - if you have kidney disease

WHEN USING

When using this product - do not use on broken skin - stop use if rash or irritation occurs

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.

DOSAGE & ADMINISTRATION

Directions

Shake well and apply evenly to underarms only

Use daily as needed

INACTIVE INGREDIENT

Inactive Ingredients

Water, PEG-40 Stearate, Cetyl Alcohol,

Isodecyl Oleate, Mineral Oil, Magnesium Aluminum Silicate, Glyceryl Stearate,

Methylparaben, Fragrance, Propylparaben, Trisodium HEDTA, Sorbic Acid

PRINCIPAL DISPLAY PANEL

New and Improved
Tussy
Antiperspirant and Deodorant

Original Fresh Spice
pH Balanced
1.7 FL. OZ (50.2 mL)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TUSSY ANTIPERSPIRANT AND DEODORANT ORIGINAL FRESH SPICE 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50481-3201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	190 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
MINERAL OIL (UNII: T5L8T28FGP)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
TRISODIUM HEDTA (UNII: K3E0U7O8KI)
SORBIC ACID (UNII: X045WJ989B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50481-3201-1	50.2 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/27/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/27/2010

Labeler - KCM Brands LLC (833150472)

Registrant - Suite K Value Added Services LLC (828385844)

Establishment
Name	Address	ID/FEI	Business Operations
Suite K Value Added Services LLC		036822144	manufacture(50481-3201)