ORALINE-SECURE CLEAR ANTIPERSPIRANT/DEODORANT- aluminum chlorohydrate gel

OraLine-Secure by

Drug Labeling and Warnings

OraLine-Secure by is a Otc medication manufactured, distributed, or labeled by J.M. Murray Center Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient:

Drug Facts

Active Ingredient:

Aluminum Chlorohydrate, 10%

Purpose:

Antiperspirant

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.

Use:

Helps lessen underarm perspiration.

Warnings:

Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease.

Directions:

Apply thin layer to underarm.

Inactive Ingredients:

Aqua, Dipropylene Glycol, Peg-40 Hydrogenated Castor Oil, Polysorbate 20, Parfum, Hydroxyethylcellulose, Phenoxyethanol, Menthol, Disodium Edta.

Product Label

Distributed by OraLine, 823 NYS RT. 13, Cortland, NY 13045

No animal based ingredients.

Ora-Line Secure  net Wt. 2 oz.

CLEAR ANTIPERSPIRANT/DEODORANT

Made in China

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INGREDIENTS AND APPEARANCE

ORALINE-SECURE  CLEAR ANTIPERSPIRANT/DEODORANT
aluminum chlorohydrate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55873-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	5.67 g  in 56.7 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MENTHOL (UNII: L7T10EIP3A)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55873-021-01	56.7 g in 1 CONTAINER; Type 0: Not a Combination Product	05/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	05/01/2014

Labeler - J.M. Murray Center Inc. (071601108)

Registrant - J.M. Murray Center Inc. (071601108)

Establishment
Name	Address	ID/FEI	Business Operations
J.M. Murray Center Inc.		071601108	relabel(55873-021) , repack(55873-021)