BODY ILLUMINATING CREME SPF 15  - octinoxate and oxybenzone cream 
MD Formulation

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VitAplus body illuminating creme SPF 15

Active Ingredient                        Purpose
Octinoxote  - 7.5%                     Sunscreen
Oxybenzone- 5.0%                    Sunscreen

When using this product do not use in or near the eyes. II product gets into eyes, rinse thoroughly with water.

Warnings For external use only.

Stop use and ask a doctor if Irritation of rash appears and lasts.

If swallowed, get medical help or contact a Polson Control Center rlahl away .

Inactive ingredients Purified Waler (Aqua), Ammonium Glycolate (and) Glycolic Acid , Glycerin, C 12-15 Alkyl Benzoate, Sucrose Cocoate, Celearyt Alcohol. Glyceryl Stearate (and) PEG- tOO Stearate, Aluminum Storch Oclenylsucclnate, Dimelhlcone/Vinyl Dlmelhlcone Crosspolymer and C 12-13
Porelh-12, Polyacrylamide and CI 3-14 lsoporaffin and laureth-7, Glyceryl Stearale. C30-45 Alkyl Methlcone, Butylene Glycol (and) Palmltoyl Hydroxypropyltrlmonlum Amylopectin/Glycerin Crosspolymer (and) Ascorbic Acid (and) l ecithin, Polmlloyl HydroxypropyHrimonlum Amylopectin/-
Glycerin Crosspolymer (and) lecithin (and) Grope Seed (Vrtis Vinilera) Exlracl, Tocopheryt Acetate, Butylene Glycol (and) Morus Bombycls (Mulberry) Extract, Butylene Glycol (and) Glycyrrhiza Glabra (Ucorlce) Exlract, Hydrolyzed Silk. Polysorbale 20 (and) Retinol. Blsobolol, Allantoin Glycyrrh ellnlc Acid, BHT. Xanthon Gum. Magnesium Aluminum Sillcale, Dlsodlum EDTA. Methylparoben. Propylparaben, Dlazolldinyl Urea (and)
lodoplopynyl Butylcorbamole

Active Ingredient                        Purpose
Octinoxote  - 7.5%                     Sunscreen
Oxybenzone- 5.0%                    Sunscreen

Directions Adults and children 6 months and over: opply sunscreen liberally before sun exposure ond reapply as needed. Children under 2 years of age should use sunscreen products with a minimum SPF of 4. Children under 6 monlhs ask a doctor.

BODY ILLUMINATING CREME SPF 15  octinoxate, oxybenzone   cream

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 66078-518 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (Octinoxate) Octinoxate 7.5 g  in 100 g Oxybenzone (Oxybenzone) Oxybenzone 5.0 g  in 100 g

Inactive Ingredients Ingredient Name Strength Methylparaben

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 66078-518-33 42 CARTON In 1 CASE contains a CARTON 1 1 BOTTLE In 1 CARTON This package is contained within the CASE (66078-518-33) and contains a BOTTLE 1 80 g In 1 BOTTLE This package is contained within a CARTON and a CASE (66078-518-33)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	07/14/2003	04/06/2011

Labeler - MD Formulation (087008363)

Registrant - Harmony Labs, Inc. (105803274)

Establishment
Name	Address	ID/FEI	Operations
Harmony Labs, Inc.		105803274	manufacture, label, pack, relabel, repack

Revised: 04/2011MD Formulation