UP AND UP CREAMY DIAPER RASH - zinc oxide ointment 
TARGET CORPORATION

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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DRUG FACTS

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

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 7 DAYS.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

CHANGE WET AND SOILED DIAPERS PROMPTLY. CLEAN THE DIAPER AREA AND ALLOW TO DRY. APPLY OINTMENT LIBERALLY AS OFTEN AS REQUIRED WITH EACH DIAPER CHANGE, ESPECIALLY AT BEDTIME OR ANYTIME WHEN EXPOSURE TO WET DIAPERS MAY BE PROLONGED.

OTHER INFORMATION

STORE BETWEEN 20-25C (68-77F).

INACTIVE INGREDIENTS:

ALOE BARBADENSIS LEAF JUICE, BEESWAX, DIMETHICONE, ETHYLHEXYLGLYCERIN, FRAGRANCE (PARFUM), MAGNESIUM SULFATE, MICROCRYSTALLINE WAX, MINERAL OIL, PEG-30 DIPOLYHYDROXYSTEARATE, PETROLATUM, PHENOXYETHANOL, POTASSIUM HYDROXIDE, SORBITAN SESQUIOLEATE, TOCOPHERYL ACETATE, WATER (AQUA).

QUESTIONS?

CALL 1-800-910-6874

LABEL COPY

IMAGE OF THE LABEL

UP AND UP  CREAMY DIAPER RASH
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-332
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE13.0 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
APIS MELLIFERA (UNII: 7S82P3R43Z)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
MAGNESIUM SULFATE (UNII: DE08037SAB)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
MINERAL OIL (UNII: T5L8T28FGP)  
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
PETROLATUM (UNII: 4T6H12BN9U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-332-04113.3 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34604/23/2012
Labeler - TARGET CORPORATION (006961700)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 4/2012
Document Id: 586953e8-e15b-415d-b49e-68d71e3473c7
Set id: f8a2e3d7-18a5-47bb-9016-ba063e05b9b3
Version: 1
Effective Time: 20120424
 
TARGET CORPORATION