FDA.reportPublic FDA data

MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3

Manufacturer
Yangzhou H&R Plastic Daily Chemical Co., Ltd.
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:40:41

Label at a glance#

ProductMERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3
Active ingredientBENZETHONIUM CHLORIDE
Label structure10 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#

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.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of eye contact, flush with water.

Don't use this product on infants under 6.

Stop use and consult doctor

OTC - STOP USE SECTION

If irritation and rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label imagelabel image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1872091benzethonium chloride 0.1 % Medicated Bar SoapPSN1
1872091benzethonium chloride 0.001 MG/MG Medicated Bar SoapSCD1
1872091benzethonium chloride 0.1 % Medicated Bar SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72797-004-01MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3144 in 1 BOXSOAP1441
72797-004-01MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 375 g in 1 PACKAGESOAP751

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72797-004MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3 (BENZETHONIUM CHLORIDE) SOAP [YANGZHOU H&R PLASTIC DAILY CHEMICAL CO., LTD.]1Current NDC, 2 package rows20241207_e35e468a-1f0c-4a3f-ac6a-cd55a72f3cc2.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72797-00472797-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CALCIUM CARBONATEH0G9379FGKIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM HYDROXIDE55X04QC32IIACT
TETRASODIUM EDTAMP1J8420LUIACT
TETRASODIUM ETIDRONATECZZ9T1T1X4IACT
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 UNWARPPED ANTIBACTERIAL DEODORANT 3BENZETHONIUM CHLORIDEYangzhou H&R Plastic Daily Chemical Co., Ltd.e35e468a-1f0c-4a3f-ac6a-cd55a72f3cc22024-12-05WarningsExact identifier
ndc (package): 72797-004-01
ndc (product): 72797-004
ndc11 (package): 72797000401
spl id: 28819252-57c9-0f9c-e063-6394a90a156f
spl set id: e35e468a-1f0c-4a3f-ac6a-cd55a72f3cc2

Reported adverse events (FAERS/openFDA)#

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