Medication Guide App

Ray Defense SPF 30 Sunscreen

Dosage form: liquid
Ingredients: AVOBENZONE 2.0mL in 100mL, OCTINOXATE 7.5mL in 100mL, OCTISALATE 5.0mL in 100mL, OCTOCRYLENE 7.5mL in 100mL, OXYBENZONE 5.0mL in 100mL
Labeler: Bioelements, Inc.
NDC Code: 49825-121

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.

Ray Defense SPF 30

Active ingredients               Purpose

Avobenzone 2.0 %              Sunscreen

Octinoxate 7.5 %                Sunscreen

Octisalate 5.0 %                 Sunscreen

Octocrylene 7.5 %               Sunscreen

Oxybenzone 5.0%                Sunscreen


Uses

Helps prevent sunburn

If used as directed with other sun protection measure (see Direction) decreases the risk of skin cancer and early skin aging caused by the sun.

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

Stop use and ask a doctor if rash occurs

Warnings


For external Use only
Do not use on broken skin.
When using this product keep out of eyes. Rinse with water to remove.

Directions

Apply liberally 15 minutes before sun exposure

Use a water resistant sunscreen if swimming or sweating

Reapply at least every 2 hours

children under 6 months: Ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

limit time in the sun, especially from 10 a.m. - 2 p.m.

Wear long-sleeve shirts, pants, hats, and sunglasses

Inactive Ingredients

Allantoin, Aloe Barbadensis Leaf Extract, C12-15 Alkyl Benzoate, Camellia Sinensis (Green Tea) Leaf Extract, Caprylic/Capric Triglyceride, Carbomer, Cetyl alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Citrus Aurantium (Bitter Orange) Flower Oil, Citrus Reticulata (Tangerine) Leaf Oil, Cyclopentasiloxane, Dimethicone, Dimethiconol, Ehtylhexylglycerin, Glycerin, Glyceryl Stearate, Glycol Distearate, Isohexadecane, Lavandula Angustifolia (Lavender) Oil, PEG-100 Stearate, Polysorbate 80, Potassium Cetyl Phophate, Salvia Officinalis (Sage) Oil, Salvea Sclarea (Clary Oil), Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Sodium Hydroxide, Stearyl Alcohol, Tetrasodium EDTA,Titanium Dioxide, Tocopheryl Acetate, Water (Aqua, Eau)



Bioelements

Ray Defense SPF 30

Broad Spectrum SPF 30 Sunscreen

Moisturizes and decreases the risk of early skin aging caused by the sun when used as directed.

118 mL / 4 Fl.Oz.




RAY DEFENSE  SPF 30 SUNSCREEN
avobenzone, octinoxate, octisalate, octocrylene, oxybenzone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49825-121
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (AVOBENZONE) AVOBENZONE2.0 mL  in 100 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE7.5 mL  in 100 mL
OCTISALATE (OCTISALATE) OCTISALATE5.0 mL  in 100 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE7.5 mL  in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE5.0 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN 
ALOE VERA LEAF 
ALKYL (C12-15) BENZOATE 
GREEN TEA LEAF 
MEDIUM-CHAIN TRIGLYCERIDES 
CETYL ALCOHOL 
CHAMOMILE 
CITRUS AURANTIUM FLOWER OIL 
CITRUS RETICULATA LEAF OIL 
CYCLOMETHICONE 5 
DIMETHICONE 
DIMETHICONOL (41 MPA.S) 
ETHYLHEXYLGLYCERIN 
GLYCERIN 
GLYCERYL MONOSTEARATE 
GLYCOL DISTEARATE 
ISOHEXADECANE 
LAVENDER OIL 
PEG-100 STEARATE 
POLYSORBATE 80 
POTASSIUM CETYL PHOSPHATE 
SAGE OIL 
CLARY SAGE OIL 
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) 
SODIUM HYDROXIDE 
STEARYL ALCOHOL 
EDETATE SODIUM 
TITANIUM DIOXIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:49825-121-021 TUBE (TUBE) in 1 CARTON
1NDC:49825-121-01118 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/23/2012
Labeler - Bioelements, Inc. (174813923)
Registrant - Bioelements, Inc. (174813923)
Establishment
NameAddressID/FEIOperations
Neutraderm146224444manufacture

Revised: 03/2012
 
Bioelements, 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 combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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