Meridian Wrapped Antibacterial Deodorant Soap
FDA Label NDC 53247-139

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bob Barker Company Inc. for the product Meridian Wrapped Antibacterial Deodorant (NDC 53247-139). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredient, purpose, uses, caution, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Active Ingredient

→ Purpose

→ Uses

→ Caution

→ Otc - Do Not Use

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Principal Display Panel - 85 G Bar Cello Pack Case

Other

Drug Facts

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Uses

For washing to decrease bacteria on skin.

Caution

For external use only.

Otc - Do Not Use

Do not use this product on infants under 6.

Otc - When Using

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

Otc - Stop Use

Stop use and consult doctor if irritation and rash develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

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

Directions

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

Inactive Ingredients

Sodium Palmate/Sodium Tallowate, Calcium Carbonate, Sodium Palm Kernelate/ Sodium Cocoate, Water, Sodium Hydroxide, Sodium Chloride, Tetrasodium EDTA, Tetrasodium Etidronate, Fragrance