ATOPALM DIAPER RASH- zinc oxide cream

ATOPALM Diaper Rash by

Drug Labeling and Warnings

ATOPALM Diaper Rash by is a Otc medication manufactured, distributed, or labeled by NeoPharm Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ATOPALM Diaper Rash Cream

Active Ingredient

Zinc Oxide 10%

Purpose

Skin Protectant

Uses

• Helps treat and prevent diaper rash
• Protects chafed skin and minor irritation associated with diaper rash
• Helps seal out wetness.
  

Warnings

For external use only.

When using this product

• avoid contact with the eyes.
  

Stop use and ask a doctor if

• Conditions worsen
• symptoms last more than seven days
• symptoms clear up and occur within a few days.
  

Keep out of reach of children.

If swallowed, get medical help immediately or contact a Poison Control Center right away.

Directions

• Change wet and soiled promptly
• Cleanse the diaper area and allow to dry.
• Apply cream liberally, as often as necessary, with each diaper change, especially at bedtime or before any prolonged exposure to wet diapers.
  

Other Information

• store at 15 degrees - 30 degrees C (59 degrees - 86 degrees F)
  
• see carton flap or tube crimp for lot number and expiration date
  

Questions or information call toll free:

1-855-ATOPALM

Inactive Ingredients

WATER, WHITE PETROLATUM, LIGHT MINERAL OIL, SORBITAN SESQUILEATE, WHITE BEESWAX, TALC, STEARIC ACID, DIMETHICONE, ALOE VERA GEL, MYRISTOYL/PALMITOYL OXOSTEARAMIDE/ARACHAMIDE MEA, CHOLESTEROL, PANTHENOL, TOCOPHERYL ACETATE, BENZYL ALCOHOL, SODIUM BENZOATE, FRAGRANCE.

ATOPALM Diaper Rash Cream 2oz (

51141-0237-2)

INGREDIENTS AND APPEARANCE

ATOPALM DIAPER RASH 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51141-0237
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
WHITE WAX (UNII: 7G1J5DA97F)
TALC (UNII: 7SEV7J4R1U)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MYRISTOYL/PALMITOYL OXOSTEARAMIDE/ARACHAMIDE MEA (UNII: 1211AIM8G7)
CHOLESTEROL (UNII: 97C5T2UQ7J)
PANTHENOL (UNII: WV9CM0O67Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51141-0237-2	57 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	06/07/2012

Labeler - NeoPharm Co., Ltd (965502912)

Registrant - NeoPharm Co., Ltd (965502912)

Establishment
Name	Address	ID/FEI	Business Operations
NeoPharm Co., Ltd		631101883	manufacture