Meridian® Unwrapped antibacterial deodorant soap

Meridian Unwrapped antibacterial deodorant by

Drug Labeling and Warnings

Meridian Unwrapped antibacterial deodorant by is a Otc medication manufactured, distributed, or labeled by Bob Barker Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT- benzethonium chloride soap 
Bob Barker Company Inc.

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Meridian® Unwrapped antibacterial deodorant soap

Drug Facts

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Uses

For washing to decrease bacteria on skin.

Caution

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 consult doctor if irritation and rash develops.

Keep out of reach of children.

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

Directions

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

Inactive Ingredients

Sodium Palmate, Calcium Carbonate, Water, Sodium Palm Kernelate, Talc, Palm Acid, Glycerin, Sodium Chloride, Sodium Laureth Sulfate, Titanium Dioxide, Palm Kernel Acid, Fragrance, Tetrasodium EDTA, Tetrasodium Etidronate

PRINCIPAL DISPLAY PANEL - 144 Bar Case

meridian®

ITEM: UWA3
DESCRIPTION: MERIDIAN® UNWRAPPED ANTIBACTERIAL DEODORANT SOAP #3
SIZE: #3
QUANTITY: 144 BARS / NET WT 2.6 OZ (75 g) PER BAR
PO # _______
CARTON # ________ OF _______
MFG DATE: _______
EXP DATE: ______
MADE IN MALAYSIA

MANUFACTURED EXCLUSIVELY FOR BOB BARKER COMPANY, INC.
7925 PURFOY RD., FUQUAY VARINA, NC 27526

BULK SHIPMENT NOT FOR RETAIL
ITEM: UWA3
SIZE: #3

PRINCIPAL DISPLAY PANEL - 144 Bar Case
MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT 
benzethonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 53247-135
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)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
TALC (UNII: 7SEV7J4R1U)  
PALM ACID (UNII: B6G0Y5Z616)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
PALM KERNEL ACID (UNII: 79P21R4317)  
EDETATE SODIUM (UNII: MP1J8420LU)  
ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 53247-135-011000 in 1 CASE09/01/201911/13/2025
111 g in 1 APPLICATOR; Type 0: Not a Combination Product
2NDC: 53247-135-02500 in 1 CASE09/01/201911/13/2025
232 g in 1 APPLICATOR; Type 0: Not a Combination Product
3NDC: 53247-135-03144 in 1 CASE09/01/201911/13/2025
375 g in 1 APPLICATOR; Type 0: Not a Combination Product
4NDC: 53247-135-04200 in 1 CASE09/01/201911/13/2025
485 g in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH DRUGM00309/01/201911/13/2025
Labeler - Bob Barker Company Inc. (058525536)

Revised: 8/2024