DYNAMIC SKIN RECOVERY SPF30  - avobenzone, octinoxate, oxybenzone and octisalate lotion 
PureTek Corporation

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active ingredients:

Avobenzone (3.0%), Octinoxate (7.5%), Octisalate (5.0%), Oxybenzone (5.0%).

other ingredients:

Water (Aqua), Octyldodecyl Neopentanoate, Butylene Glycol, Pentylene Glycol, Arachidyl Alcohol, Behenyl Alcohol, Nylon-12, Leuconostoc/Radish Root Ferment Filtrate, Arginine/Lysine Polypeptide, Pamlitoyl Tripeptide-5, Camellia Sinensis Leaf Extract, Arachidyl Glycoside, Glycine Soja (Soybean) Protein, Sodium Hyaluronate, Saccharomyces Lysate Extract, Oenothera Biennis (Evening Primrose) Oil, Glucosamine HCl, Allantoin, Squalane, Algae Extract, Yeast Extract, Chrysanthemim Parthenium (Feverfew) Extract, Colloidal Oatmeal, Urea, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polysorbate 60, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Disodium EDTA, Citronellol, Eugenol, Geraniol, Limonene, Linalool, Helianthus Annuus (Sunflower) Seed Oil, Rose Flower Oil, Citrus Medica Limonum (Lemon) Peel Oil, Pelargonium Graveolens Oil, Citrus Medica Limonum (Lemon) Peel Extract, Eugenia Caryophyllus (Clove) Flower Oil, Pelargonium Groveolens Flower Oil, Aniba Rosaeodora (Rosewood) Wood Oil, Caprylic/Capric Triglyceride,Titanium Dioxide (Cl 77891). 

directions:

Apply to face and neck, preferably 30 minutes prior to daylight exposure.

warnings:

For external use only, not to be swallowed. Avoid contact with eyes. If contact occurs, flush thoroughly with water. Apply prior to sun exposure. Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner. Do not use on infants under 6 months old. Contains Oxybenzone.

Label

DYNAMIC SKIN RECOVERY SPF30  avobenzone, octinoxate, octisalate, oxybenzone   lotion

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 59088-856 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (AVOBENZONE) AVOBENZONE 30 uL  in 1 mL OCTINOXATE (OCTINOXATE) OCTINOXATE 75 uL  in 1 mL OXYBENZONE (OXYBENZONE) OXYBENZONE 5 uL  in 1 mL OCTISALATE (OCTISALATE) OCTISALATE 5 uL  in 1 mL

Inactive Ingredients Ingredient Name Strength WATER   OCTYLDODECYL NEOPENTANOATE   BUTYLENE GLYCOL   PENTYLENE GLYCOL   ARACHIDYL ALCOHOL   DOCOSANOL   ALLANTOIN   HYALURONATE SODIUM   SACCHAROMYCES LYSATE   EVENING PRIMROSE OIL   GLUCOSAMINE HYDROCHLORIDE   SQUALANE   YEAST   UREA   PALMITOYL TRIPEPTIDE-5   GREEN TEA LEAF   OATMEAL   MEDIUM-CHAIN TRIGLYCERIDES   POLYSORBATE 60   GLYCERIN   EDETATE DISODIUM   .BETA.-CITRONELLOL, (R)-   EUGENOL   GERANIOL   LIMONENE, (+/-)-   LINALOOL, DL-   SUNFLOWER OIL   ROSA DAMASCENA FLOWER OIL   LEMON OIL   ARACHIDYL GLUCOSIDE   LEMON PEEL   CLOVE OIL   PELARGONIUM GRAVEOLENS FLOWER OIL   ROSEWOOD OIL   TITANIUM DIOXIDE   FEVERFEW   COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE   ROSE OIL   GERANIUM OIL, ALGERIAN TYPE   LEMON

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 59088-856-04 50 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	03/01/2009

Labeler - PureTek Corporation (785961046)

Establishment
Name	Address	ID/FEI	Operations
PureTek Corporation		785961046	manufacture, label, pack, outsourcing human drug compounding, relabel, repack

Establishment
Name	Address	ID/FEI	Operations
PureTek Corporation		031678746	manufacture, label, pack, outsourcing human drug compounding, relabel, repack

Revised: 05/2011PureTek Corporation