BOB BARKER ANTIBACTERIAL UNWRAPPED BODY- benzethonium chloride soap

Bob Barker Antibacterial unwrapped body by

Drug Labeling and Warnings

Bob Barker Antibacterial unwrapped body by is a Otc medication manufactured, distributed, or labeled by Bob Barker Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Uses

For washing to decrease bacteria on skin.

Warnings

For External Use Only.

Do not use this product on infants under 6.

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

Stop use and ask doctor if irritation and redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet bar with water
• Lather vigorously and wash skin
• Rinse and dry thoroughly

Inactive Ingredients

Soap (Sodium Palmate and/or Sodium Tallowate, Sodium Cocoate and/or Sodium Palm Kernelate), Calcium Carbonate, Water, Glycerin, Sodium Chloride, Sodium Hydroxide, Fragrance, Tetrasodium EDTA, Etidronate Tetrasodium

PRINCIPAL DISPLAY PANEL - 500 Bar Case

BobBarker®

ANTIBACTERIAL UNWRAPPED BODY SOAP

500 Bars-Total Net Weight 564.38 OZ. (35.27 LB) (16 KG)

INGREDIENTS AND APPEARANCE

BOB BARKER ANTIBACTERIAL UNWRAPPED BODY 
benzethonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53247-113
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Sodium Palmate (UNII: S0A6004K3Z)
Sodium Tallowate, Beef (UNII: 07RIK6QMEW)
Sodium Cocoate (UNII: R1TQH25F4I)
Sodium Palm Kernelate (UNII: 6H91L1NXTW)
Calcium Carbonate (UNII: H0G9379FGK)
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Sodium Chloride (UNII: 451W47IQ8X)
Sodium Hydroxide (UNII: 55X04QC32I)
Edetate Sodium (UNII: MP1J8420LU)
Etidronate Tetrasodium (UNII: CZZ9T1T1X4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53247-113-01	1000 in 1 CASE	06/01/2017
1		11 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53247-113-02	500 in 1 CASE	06/01/2017
2		32 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53247-113-03	144 in 1 CASE	06/01/2017
3		75 g in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 53247-113-04	200 in 1 CASE	06/01/2017
4		85 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 NOT FINAL	part333E	06/01/2017

Labeler - Bob Barker Company Inc. (058525536)