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

PRINCIPAL DISPLAY PANEL - 75 g Bar Case Label

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 CHINA

BULK SHIPMENT NOT FOR RETAIL

ITEM: UWA3
SIZE: #3

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

INGREDIENTS AND APPEARANCE

MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT 
benzethonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53247-142
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: 53247-142-01	1000 in 1 CASE	01/01/2025
1		11 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53247-142-02	500 in 1 CASE	01/01/2025
2		32 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53247-142-03	144 in 1 CASE	01/01/2025
3		75 g in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 53247-142-04	144 in 1 CASE	01/01/2025
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	01/01/2025

Labeler - Bob Barker Company Inc. (058525536)