K-mom Baby Tooth
FDA Label NDC 73429-0002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mother-k Co.,ltd for the product K-mom Baby Tooth (NDC 73429-0002). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

For dental care

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Use as small amount as a grain of rice.

Warnings

Keep away from infants.

Inactive Ingredient

Sorbitol, Water, Xylitol, Stevioside, Cellulose Gum, Xanthan Gum, Potassium Sorbate, Etc.

Dosage & Administration

For dental use only

Package Label.Principal Display Panel

1 (Label Baby)

1 (Label Baby)

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