PROTEX COMPLETE ANTIBACTERIAL BAR- chloroxylenol soap

Protex Complete Antibacterial Bar by

Drug Labeling and Warnings

Protex Complete Antibacterial Bar by is a Otc medication manufactured, distributed, or labeled by Colgate-Palmolive Company, HADA International S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial

Use

Helps reduce bacteria that potentially can cause disease

Warnings

For external use only.

When using this product, avoid contact with eyes. In case of contact, flush with water.

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

Directions

Wet bar with water. Lather and wash skin. Rinse and dry thoroughly.

Inactive ingredients

Sodium Laurate/Linoleate/Oleate/Palmitate, Water, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Etidronic Acid, Titanium Dioxide.

Questions?

1-800-443-0602

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DIST. BY:
COLGATE-PALMOLIVE COMPANY, NEW YORK, NY 10022 USA

PRINCIPAL DISPLAY PANEL - 104.8 g Applicator Carton

NEW
Eliminates 99.9% of bacteria*

Protex®
For the Good Health of your Skin
COMPLETE

Antibacterial

Antibacterial Bar Soap
NET WT 3.7 OZ (104.8 g)

INGREDIENTS AND APPEARANCE

PROTEX COMPLETE ANTIBACTERIAL BAR 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 35000-069
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURATE (UNII: K146MR5EXO)
SODIUM LINOLEATE (UNII: 872C9A1W9I)
SODIUM OLEATE (UNII: 399SL044HN)
SODIUM PALMITATE (UNII: JQ43KP6296)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
ETIDRONIC ACID (UNII: M2F465ROXU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 35000-069-01	1 in 1 CARTON	12/01/2021
1		104.8 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 35000-069-03	3 in 1 CELLO PACK	12/01/2021
2		1 in 1 CARTON
2		104.8 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 35000-069-06	6 in 1 CELLO PACK	12/01/2021
3		1 in 1 CARTON
3		104.8 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH DRUG	505G(a)(3)	12/01/2021

Labeler - Colgate-Palmolive Company (001344381)

Establishment
Name	Address	ID/FEI	Business Operations
HADA International S.A.		882405152	MANUFACTURE(35000-069)