BUDPAK DIAPER RASH- zinc oxide cream 
Budpak Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Budpak Diaper Rash Cream

Active Ingredient

Zinc Oxide 13%

Purpose

Skin Protectant

Uses

Helps treat and prevent diaper rash. Protects chafed skin due to diaper rash. Helps seal out wetness

Warnings

For external use only

When using this product do not get into eyes

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

Keep out of reach of children.

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

Directions

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

Other Information

Store at 20°to 25°C (68° to 77°F).

Inactive Ingredients

Water, Mineral Oil, Petrolatum, Beeswax, Dimethicone, Sorbitan Sesquioleate, Microcrystalline Wax, PEG-30 Dipolyhydroxystearate, Magnesium Sulfate, Phenoxyethanol, Methylparaben, Fragrance, Potassium Hydroxide, Propylparaben, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.

PRINCIPAL DISPLAY PANEL

Budpak Diaper Rash Cream

Zinc Oxide 13%

NET WT 1 OZ (28 g)

image of package label

BUDPAK DIAPER RASH 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:27293-028
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
MAGNESIUM SULFATE (UNII: DE08037SAB)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:27293-028-141 in 1 BOX
114 g in 1 TUBE
2NDC:27293-028-281 in 1 BOX
228 g in 1 TUBE
3NDC:27293-028-351 in 1 BOX
335 g in 1 TUBE
4NDC:27293-028-421 in 1 BOX
442 g in 1 TUBE
5NDC:27293-028-021 in 1 BOX
5113 g in 1 TUBE
6NDC:27293-028-031 in 1 BOX
6226 g in 1 TUBE
7NDC:27293-028-04453 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34702/14/2014
Labeler - Budpak Inc. (183224849)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
NameAddressID/FEIBusiness Operations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(27293-028)

Revised: 2/2014
Document Id: 985046ac-f4ae-4c7a-881d-c2491a3a0f6a
Set id: 15c427f3-09a8-4514-b95a-cf966c574f3a
Version: 1
Effective Time: 20140214
 
Budpak Inc.