Bob Barker® Antibacterial unwrapped body 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]

BOB BARKER ANTIBACTERIAL UNWRAPPED BODY- benzethonium chloride soap 
Bob Barker Company Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Bob Barker® Antibacterial unwrapped body soap

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), Water, Palm Acid, Glycerin, Sodium Chloride, Coconut Acid, Fragrance, Tetrasodium EDTA, Citric Acid Anhydrous

PRINCIPAL DISPLAY PANEL - 1000 Bar Case

BobBarker®

ANTIBACTERIAL UNWRAPPED BODY SOAP

1000 Bars-Total Net Weight 409.18 OZ. (25.57 LB) (11.6 KG)

PRINCIPAL DISPLAY PANEL - 1000 Bar Case
BOB BARKER ANTIBACTERIAL UNWRAPPED BODY 
benzethonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 53247-106
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Sodium Palmate (UNII: S0A6004K3Z)  
Sodium Tallowate, Beef (UNII: 07RIK6QMEW)  
Sodium Cocoate (UNII: R1TQH25F4I)  
Sodium Palm Kernelate (UNII: 6H91L1NXTW)  
Water (UNII: 059QF0KO0R)  
Palm Acid (UNII: B6G0Y5Z616)  
Glycerin (UNII: PDC6A3C0OX)  
Sodium Chloride (UNII: 451W47IQ8X)  
Coconut Acid (UNII: 40U37V505D)  
Edetate Sodium (UNII: MP1J8420LU)  
Anhydrous Citric Acid (UNII: XF417D3PSL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 53247-106-011000 in 1 CASE01/01/201712/26/2019
111.6 g in 1 APPLICATOR; Type 0: Not a Combination Product
2NDC: 53247-106-02500 in 1 CASE01/01/201712/26/2019
235.44 g in 1 APPLICATOR; Type 0: Not a Combination Product
3NDC: 53247-106-03144 in 1 CASE01/01/201712/26/2019
381.04 g in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/201712/26/2019
Labeler - Bob Barker Company Inc. (058525536)

Revised: 12/2019
Document Id: 4c23ab4c-2696-4406-8835-087455de5d68
Set id: eb591828-3dbe-4684-9b67-c132638239e3
Version: 2
Effective Time: 20191227
 
Bob Barker Company Inc.