BABY MAGIC DIAPER RX- zinc oxide cream

Baby Magic Diaper Rx by

Drug Labeling and Warnings

Baby Magic Diaper Rx by is a Otc medication manufactured, distributed, or labeled by Naterra International INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient : Zinc Oxide (28%)

PURPOSE

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

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.

PRINCIPAL DISPLAY PANEL

DOSAGE & ADMINISTRATION

Enter section text here

INGREDIENTS AND APPEARANCE

BABY MAGIC DIAPER RX  
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 45765-5130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	23.8 g  in 85 g

Inactive Ingredients
Ingredient Name	Strength
Allantoin (UNII: 344S277G0Z)
Ascorbyl Palmitate (UNII: QN83US2B0N)
YELLOW WAX (UNII: 2ZA36H0S2V)
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
SAFFLOWER OIL (UNII: 65UEH262IS)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
AVOCADO OIL (UNII: 6VNO72PFC1)
Petrolatum (UNII: 4T6H12BN9U)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
Tocopherol (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 45765-5130-0	85 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	04/30/2010

Labeler - Naterra International INC. (879056786)