MERIDIAN ANTIBACTERIAL DEODORANT- benzethonium chloride soap

Meridian Antibacterial Deodorant by

Drug Labeling and Warnings

Meridian Antibacterial Deodorant by is a Otc medication manufactured, distributed, or labeled by Yangzhou Hongshengding Chemical Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Use

For washing to decrease bacteria on skin

Warnings

For external use only

Do not use this product on infants under 6

WHEN USING

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

Stop use and consult a doctor if irritation and rash develop

KEEP OUT OF REACH OF CHILDREN

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MERIDIAN ANTIBACTERIAL DEODORANT 
benzethonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71035-004
Route of Administration	TOPICAL

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)
WATER (UNII: 059QF0KO0R)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
CALCIUM CARBONATE (UNII: H0G9379FGK)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE SODIUM (UNII: MP1J8420LU)
TETRASODIUM ETIDRONATE (UNII: CZZ9T1T1X4)
SODIUM TALLOWATE (UNII: 07RIK6QMEW)
SODIUM COCOATE (UNII: R1TQH25F4I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71035-004-02	500 in 1 CARTON	07/27/2025
1		1 in 1 POUCH
1		32 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 71035-004-03	144 in 1 CARTON	07/27/2025
2		1 in 1 POUCH
2		75 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 71035-004-04	144 in 1 CARTON	07/27/2025
3		1 in 1 POUCH
3		85 g in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 71035-004-01	1000 in 1 CARTON	07/27/2025
4		1 in 1 POUCH
4		11 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	M005	07/27/2025

Labeler - Yangzhou Hongshengding Chemical Co.,Ltd. (543774755)

Establishment
Name	Address	ID/FEI	Business Operations
Yangzhou Hongshengding Chemical Co.,Ltd.		543774755	manufacture(71035-004)