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wet n wild Ultimate Match

Dosage form: liquid
Ingredients: OCTINOXATE 6mL in 100mL, OXYBENZONE 2mL in 100mL
Labeler: Markwins Beauty Products, Inc
NDC Code: 12027-102

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.

Active Ingredients
Octinoxate 6%
Oxybenzone 2%

Use• Helps prevent sunburn

Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or skin aging.

For external use only.

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor
if rash occurs

Keep out of reach of children.
If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions • apply liberally 15 minutes before sun exposure • reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• children under 6 months: Ask a doctor

Inactive Ingredients/Ingredients inactifs Water/Eau, Tridecyl Trimellitate, Talc, Isopropyl Myristate, Isododecane, Butylene Glycol, Glycerin, Glyceryl Stearate SE, Sorbitan Sesquioleate, Triacontanyl PVP, Triethanolamine, Stearic Acid, Cetyl Palmitate, Alumina, Sodium Laureth Sulfate, Chlorphenesin, Hydroxyethylcellulose, Acrylates Copolymer, Tocopheryl Acetate, Dipotassium Glycyrrhizate, Disodium EDTA, Xanthan Gum, Caprylic/Capric Triglyceride, Stearyl Glycyrrhetinate, Laminaria Ochroleuca Extract, Sodium Hyaluronate, Methylisothiazolinone
(MAY CONTAIN/PEUT CONTENIR): Iron Oxides/CI 77491, CI 77492, CI 77499, Titanium Dioxide/CI 77891, Ultramarines/CI 77007 77891, Yellow 6 Lake/CI 15985, Yellow 10 Lake/CI 47005, Zinc Oxide/CI 77947)

Package Label

WET N WILD  ULTIMATE MATCH
octinoxate oxybenzone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12027-102
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE6 mL  in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE2 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
TRIDECYL TRIMELLITATE 
TALC 
ISOPROPYL MYRISTATE 
ISODODECANE 
BUTYLENE GLYCOL 
GLYCERIN 
GLYCERYL MONOSTEARATE 
SORBITAN SESQUIOLEATE 
TRIACONTANYL PVP (WP-660) 
TROLAMINE 
STEARIC ACID 
CETYL PALMITATE 
ALUMINUM OXIDE 
SODIUM LAURETH SULFATE 
CHLORPHENESIN 
DISODIUM GLYCYRRHIZATE 
EDETATE DISODIUM 
XANTHAN GUM 
STEARYL GLYCYRRHETINATE 
LAMINARIA OCHROLEUCA 
HYALURONATE SODIUM 
METHYLISOTHIAZOLINONE 
FERRIC OXIDE RED 
TITANIUM DIOXIDE 
Packaging
#Item CodePackage Description
1NDC:12027-102-2929.6 mL in 1 BOTTLE, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35212/01/2011
Labeler - Markwins Beauty Products, Inc (135407760)
Establishment
NameAddressID/FEIOperations
Markwins International Corp.544845621manufacture

Revised: 11/2011
Document Id: a3085dad-4a66-4505-9f09-0030441a6dfe
Set id: 4a5e9b5d-3b58-4483-bdfe-27e73870c071
Version: 1
Effective Time: 20111119
 
Markwins Beauty Products, Inc

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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