FDA.reportPublic FDA data

Meridian Unwrapped Antibacterial Deodorant

Manufacturer
Yangzhou Hongshengding Chemical Co.,Ltd.
Effective date
2025-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:08:47

Label at a glance#

ProductMeridian Unwrapped Antibacterial Deodorant
Active ingredientBENZETHONIUM CHLORIDE
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only

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

Stop use and consult a doctor if irritation and rash develop

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

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71035-003-01Meridian Unwrapped Antibacterial Deodorant1000 in 1 CARTONSOAP10001
71035-003-01Meridian Unwrapped Antibacterial Deodorant11 g in 1 APPLICATORSOAP111
71035-003-02Meridian Unwrapped Antibacterial Deodorant32 g in 1 APPLICATORSOAP321
71035-003-02Meridian Unwrapped Antibacterial Deodorant500 in 1 CARTONSOAP5001
71035-003-03Meridian Unwrapped Antibacterial Deodorant144 in 1 CARTONSOAP1441
71035-003-03Meridian Unwrapped Antibacterial Deodorant75 g in 1 APPLICATORSOAP751
71035-003-04Meridian Unwrapped Antibacterial Deodorant85 g in 1 APPLICATORSOAP851
71035-003-04Meridian Unwrapped Antibacterial Deodorant144 in 1 CARTONSOAP1441

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71035-00371035-003-02, 71035-003-03, 71035-003-04, 71035-003-01

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
NameUNIIKind
SODIUM PALMATES0A6004K3ZIACT
WATER059QF0KO0RIACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
CALCIUM CARBONATEH0G9379FGKIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE SODIUMMP1J8420LUIACT
TETRASODIUM ETIDRONATECZZ9T1T1X4IACT
SODIUM TALLOWATE07RIK6QMEWIACT
SODIUM COCOATER1TQH25F4IIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Meridian Unwrapped Antibacterial DeodorantBENZETHONIUM CHLORIDEYangzhou Hongshengding Chemical Co.,Ltd.a2b9570f-312c-4f46-994d-efe057b247aa2025-07-28WarningsExact identifier
ndc (package): 71035-003-04
ndc (package): 71035-003-02
ndc (package): 71035-003-01
ndc (package): 71035-003-03
ndc (product): 71035-003
ndc11 (package): 71035000303
ndc11 (package): 71035000304
ndc11 (package): 71035000301
ndc11 (package): 71035000302
spl id: 3afb56f6-8695-dfcd-e063-6394a90aa566
spl set id: a2b9570f-312c-4f46-994d-efe057b247aa

Reported adverse events (FAERS/openFDA)#

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