Meridian Unwrapped antibacterial deodorant

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Meridian Unwrapped antibacterial deodorant
Generic name: BENZETHONIUM CHLORIDE
Manufacturer: Bob Barker Company Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c2d13d97-99ce-4a24-bdd6-684fbbf242a4
SPL ID: 19e90d08-316a-4f1e-b1a7-0aaaa4faea15
Version: 3
Effective date: 2026-07-29
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:15:14

Harmonized routes table
Harmonized routes
CUTANEOUS

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Meridian Unwrapped antibacterial deodorant	openfda.brand_name
generic name		BENZETHONIUM CHLORIDE	openfda.generic_name
manufacturer name		Bob Barker Company Inc.	openfda.manufacturer_name
ndc	package	53247-142-03	openfda.package_ndc
ndc	package	53247-142-01	openfda.package_ndc
ndc	package	53247-142-02	openfda.package_ndc
ndc	package	53247-142-04	openfda.package_ndc
ndc	product	53247-142	openfda.product_ndc
ndc11	package	53247014201	derived:openfda.package_ndc
ndc11	package	53247014203	derived:openfda.package_ndc
ndc11	package	53247014204	derived:openfda.package_ndc
ndc11	package	53247014202	derived:openfda.package_ndc
rxcui		1872091	openfda.rxcui
spl id		19e90d08-316a-4f1e-b1a7-0aaaa4faea15	id
spl set id		c2d13d97-99ce-4a24-bdd6-684fbbf242a4	set_id
unii		PH41D05744	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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