Moisture Barrier
FDA Label NDC 43749-231

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Unipack Llc for the product Moisture Barrier (NDC 43749-231). 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 active ingredient, purpose, uses, warnings, do not use on, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Active Ingredient

White Petrolatum 98.3%

Purpose

Skin Protectant

Uses

Temporarily protects minor cuts, scrapes, and burns

Temporarily protects and helps relieve chapped or cracked skin

Helps treat and prevent diaper rash caused from wetness, urine and/or stool

Warnings

For external use only

Do Not Use On

Do not use on - deep or puncture wounds - animal bites - serious burns - an area that is infected

When Using This Product

When using this product - do not get into eyes

Stop Use And Ask A Doctor If

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

Keep Out Of Reach Of Children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Gently cleanse and pat dry affected area

Apply as needed

Inactive Ingredients

aloe extract, benzethonium chloride, cholecalciferol (vitamin D), cococaprylate / caprate, corn oil, retinyl palmitate (vitamin A), tocopheryl acetate (vitamin E).

Other Information

Protect from freezing.  Avoid excessive heat.

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