Baby Magic Diaper Rx
FDA Label NDC 45765-5130

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Naterra International Inc. for the product Baby Magic Diaper Rx (NDC 45765-5130). 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, warnings, indications & usage, inactive ingredient, package label.principal display panel, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient : Zinc Oxide (28%)


Otc - Purpose

Uses: Helps treat and prevent diaper rash , chaged skin and minor skin irritation by protecting and ealing out wetness.


Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or cntact a Poison Control Center right away


Warnings

Warnings; For external use only


Indications & Usage

Direction

Change wet and soiled diapers promptly; cleanse diaper area and allow to dry

Apply product liberally with each diaper change and expecially at bedtime when exposure to wet diapers may be prolonged


Inactive Ingredient

Allantoin ,Ascorbyl Palmitate , Beeswax , BHA , Carthamus Tintorius (Safflower) Seed Oil , Fragrance , Glycyrrhiza Glabra (Licorice) Root Extract ,

Persea Gratissima (Avocado) Oil , Petrolatum , Retinyl Palmitate , Tocopherol , Tocopheryl Acetate.


Dosage & Administration

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