Bathscriptions Daily Moisturizing
FDA Label NDC 70990-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Donegal Bay Ltd for the product Bathscriptions Daily Moisturizing (NDC 70990-001). 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, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient:

Dimethicone 2.0%

Otc - Purpose

Purpose:

Skin Protectant

Indications & Usage

Uses:

Helps prevent and temporarily protects chafted, chapped or cracked skin. Helps prevent and protect from the drying effect of wind and cold weather

Warnings

Warnings:

For external use only

When using this product, do not get into eyes

Otc - Stop Use

Stop use and ask a doctor if condition worsens or if symptoms last for more than 7 days or clear up and occur again within a few days

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

Dosage & Administration

Direction:

Apply as needed

Inactive Ingredient

Inactive Ingredients:

Water, Isopropyl Palmitate, Avena sativa (Oat) Flour, Cetyl Alcohol, Glycerin, Distearyldimonium Chloride, Benzyl Alcohol, Sodium Chloride

Package Label.Principal Display Panel

Image Description (Dailymoisturizinglotion)

Image Description (Dailymoisturizinglotion)

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