MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT- benzethonium chloride 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]

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT 
benzethonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53247-135
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)
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53247-135-01	1000 in 1 CASE	09/01/2019
1		11 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53247-135-02	500 in 1 CASE	09/01/2019
2		32 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53247-135-03	144 in 1 CASE	09/01/2019
3		75 g in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 53247-135-04	200 in 1 CASE	09/01/2019
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 drug	M003	09/01/2019

Labeler - Bob Barker Company Inc. (058525536)