Meridian

Manufacturer: Bob Barker Company Inc. | Yangzhou Jyr daily chemical Co., Ltd | Yangzhou Safepure Daily Chemical Cleaning Products Co.,ltd.
Effective date: 2026-07-29
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-08-01 05:10:10

Label at a glance#

ProductMeridian Unwrapped antibacterial deodorant

Active ingredientBENZETHONIUM CHLORIDE

Label structure8 sections

Indications and uses

For washing to decrease bacteria on skin.

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on skin.

Caution

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use this product on infants under 6.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and consult doctor if irritation and rash develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

(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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Principal Display Panel - 75 g Bar Case Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Meridian Unwrapped antibacterial deodorant
BENZETHONIUM CHLORIDE
BENZETHONIUM
SODIUM PALMATE
SODIUM TALLOWATE, BEEF
SODIUM COCOATE
SODIUM PALM KERNELATE
CALCIUM CARBONATE
WATER
GLYCERIN
SODIUM CHLORIDE
SODIUM HYDROXIDE
EDETATE SODIUM
ETIDRONATE TETRASODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53247-142	53247-142-01, 53247-142-02, 53247-142-03, 53247-142-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZETHONIUM CHLORIDE	PH41D05744	ACTIB
SODIUM PALMATE	S0A6004K3Z	IACT
SODIUM TALLOWATE, BEEF	07RIK6QMEW	IACT
SODIUM COCOATE	R1TQH25F4I	IACT
SODIUM PALM KERNELATE	6H91L1NXTW	IACT
CALCIUM CARBONATE	H0G9379FGK	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ETIDRONATE TETRASODIUM	CZZ9T1T1X4	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2025-07-21	daily-update	2026-06-12 05:10:15
1	2025-07-21	full-release	2026-06-01 01:08:10

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meridian Unwrapped antibacterial deodorant	BENZETHONIUM CHLORIDE	Bob Barker Company Inc.	c2d13d97-99ce-4a24-bdd6-684fbbf242a4	2026-07-29	Warnings	Exact identifier ndc (package): 53247-142-03 ndc (package): 53247-142-01 ndc (package): 53247-142-02 ndc (package): 53247-142-04 ndc (product): 53247-142 ndc11 (package): 53247014201 ndc11 (package): 53247014203 ndc11 (package): 53247014204 ndc11 (package): 53247014202 spl id: 19e90d08-316a-4f1e-b1a7-0aaaa4faea15 spl set id: c2d13d97-99ce-4a24-bdd6-684fbbf242a4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.