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Absolute Total BB SPF37 PA 3Plus

Dosage form: cream
Ingredients: TITANIUM DIOXIDE 3.6g in 40g, ZINC OXIDE 2.52g in 40g, ARBUTIN 0.8g in 40g, ADENOSINE 0.016g in 40g
Labeler: WIZCOZ CORPORATION LTD
NDC Code: 49715-011

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.

Purpose: Sunscreen

Active Ingredients: Titanium Dioxide 9.01%, Zinc Oxide 6.30%, Arbutin 2%, Adenosine 0.04%

When using this product: Do not use other than directed

Do Not Use: On wounds, rashes, dermatitis or damaged skin

Keep Out of Reach of Children: If swallowed, get medical help or contact a Poison Control Center immediately

Stop Use: Please stop using this product and contact a dermatologist.
                1. If red rash, swelling, itch or irritation occurs
                2. If direct sunlight affects the area as above

Warnings: For external use only.  Do not use other than directed.  Keep the lid back on after using

Storage: Keep in a cool, dry place away from heat and direct sunlight

Direction:  
Step 1: Clean and dry your face
Step 2: Use the basic skincare products
Step 3: Use small amount of it and apply evenly and thoroughly to your face
                

Inactive Ingredients: Chlorphenesin, Propylparaben

ABSOLUTE TOTAL BB SPF37 PA 3PLUS 
titanium dioxide, zinc oxide, arbutin, adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49715-011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE3.6 g  in 40 g
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE2.52 g  in 40 g
ARBUTIN (ARBUTIN) ARBUTIN0.8 g  in 40 g
ADENOSINE (ADENOSINE) ADENOSINE0.016 g  in 40 g
Inactive Ingredients
Ingredient NameStrength
PROPYLPARABEN 
CHLORPHENESIN CARBAMATE 
Packaging
#Item CodePackage Description
1NDC:49715-011-4040 g in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35212/01/2011
Labeler - WIZCOZ CORPORATION LTD (690397273)
Registrant - WIZCOZ CORPORATION LTD (690397273)
Establishment
NameAddressID/FEIOperations
WIZCOZ CORPORATION LTD690397273manufacture

Revised: 12/2011
Document Id: 48208893-0350-453a-aa5a-de1fa6673ec8
Set id: 2836734d-bde8-4e12-89e7-2ef429e12906
Version: 1
Effective Time: 20111201
 
WIZCOZ CORPORATION LTD

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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