Meridian Wrapped 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 Wrapped antibacterial deodorant
Generic name: BENZETHONIUM CHLORIDE
Manufacturer: Bob Barker Company Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 84aada12-f26e-4dc9-a256-8746c6431f61
SPL ID: 73d444c9-a051-4bfc-996b-d0ce46436ef2
Version: 1
Effective date: 2025-07-15
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:25:59

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 Wrapped antibacterial deodorant	openfda.brand_name
generic name		BENZETHONIUM CHLORIDE	openfda.generic_name
manufacturer name		Bob Barker Company Inc.	openfda.manufacturer_name
ndc	package	53247-139-04	openfda.package_ndc
ndc	package	53247-139-03	openfda.package_ndc
ndc	package	53247-139-01	openfda.package_ndc
ndc	package	53247-139-02	openfda.package_ndc
ndc	product	53247-139	openfda.product_ndc
ndc11	package	53247013903	derived:openfda.package_ndc
ndc11	package	53247013901	derived:openfda.package_ndc
ndc11	package	53247013902	derived:openfda.package_ndc
ndc11	package	53247013904	derived:openfda.package_ndc
rxcui		1872091	openfda.rxcui
spl id		73d444c9-a051-4bfc-996b-d0ce46436ef2	id
spl set id		84aada12-f26e-4dc9-a256-8746c6431f61	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.