Label: DD CREAM DERMATOLOGICALLY DEFINING BB CREAM BROAD SPECTRUM SPF 30 cream
- NDC Code(s): 59735-565-01
- Packager: MANA Products, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 3, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- USE
- WARNINGS
-
DIRECTIONS
- Apply liberally 15 minutes before sun exposure
- Reapply at least every 2 hours
- Use water resistant sunscreen if swimming or sweathing
- Sun Protection Measures: Spending time in the sun decreases risk of skin cancer and early again. To decrease this risk, regulaory use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun especially from 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses.
- Children under 6 months: ask a doctor
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INACTIVE INGREDIENTS
Alumina, Aluminum Hydroxide, Behenyl Alcohol, Butylene Glycol, C12-15 Alkyl Benzoate, Caprylic/Capric/Myristic/Stearic Triglyceride, Caprylyl Glycol, Carbomer, Cellulose Gum, Cety Alcohol, Dextrin Palmitate, Dimethicone, Dimethylacrylamide/Acrylic Acid/Plystyrene Ethyl Methacylate, Disodium EDTA, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Hexylene Glycol, Hydrogenated Lecithin, Isostearic Acid, Lycium Barbarum Fruit Extract, Lysine, Magnesium Chloride, Nordihydroguaiaretic Acid, Octyldodecyl Neopenanoate, Oleanolic Acid, Palmitoyl Hexapeptide-14, Panthenol, PEG-60 Almond Glycerides, Phenoxyethanol, Phospholipids, Phytantriol, Polygleceryl-3 Diisostearate, Polysorbate 80, Potassium Chloride, Silica, Sodium Benozate, Sodium Chloride, Sodium Dehydroacetate, Sodium Hyaluronate Crosspolymer, Sodium Hydroxide, Squalane, Steareth-2, Steareth-21, Stearic Acid, Superoxide Dismutase, Tetrahexyldecyl Ascorbate, Tocopherol, Tocopheryl Acetate, Triethoxycaprylylsilane, Triethylhexanoin, Water, Xanthan Gum, Zinc Chloride May Contain (+/-): Mica, Iron Oxides.
- OTHER INFORMATION
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DD CREAM DERMATOLOGICALLY DEFINING BB CREAM BROAD SPECTRUM SPF 30
dd cream dermatologically defining bb cream broad spectrum spf 30 creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59735-565 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3.3 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 12.05 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) 2,3-DIMETHYLACRYLIC ACID, (E)- (UNII: I5792N03HC) ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO) HEXYLENE GLYCOL (UNII: KEH0A3F75J) LYSINE (UNII: K3Z4F929H6) NORDIHYDROGUAIARETIC ACID, (+/-)- (UNII: 7PZ73W4ZNR) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) PALMITOYL HEXAPEPTIDE-12 (UNII: HO4ZT5S86C) PHENOXYETHANOL (UNII: HIE492ZZ3T) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SILICON (UNII: Z4152N8IUI) SODIUM CHLORIDE (UNII: 451W47IQ8X) SQUALANE (UNII: GW89575KF9) STEARIC ACID (UNII: 4ELV7Z65AP) SUPEROXIDE DISMUTASE (CU-ZN) SACCHAROMYCES CEREVISIAE (UNII: ZQP6EKT6WD) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K) XANTHAN GUM (UNII: TTV12P4NEE) BEHENYL BEHENATE (UNII: K8NU647RJ0) CAPRYLIC/CAPRIC/PALMITIC/STEARIC TRIGLYCERIDE (UNII: ZF29F7IK5I) .ALPHA.-CELLULOSE (UNII: I355QGZ19A) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) PANTHENOL (UNII: WV9CM0O67Z) PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F) PHYTANTRIOL (UNII: 8LVI07A72W) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) ISOSTEARIC ACID (UNII: X33R8U0062) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) TOCOPHEROL (UNII: R0ZB2556P8) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ALUMINUM (UNII: CPD4NFA903) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) C12-15 ALCOHOLS (UNII: 2C8M6XLB5C) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOMER 940 (UNII: 4Q93RCW27E) CETYL ALCOHOL (UNII: 936JST6JCN) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59735-565-01 1 in 1 CARTON 12/12/2016 1 40 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/12/2016 Labeler - MANA Products, INC. (078870292) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS, INC 032870270 manufacture(59735-565) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS, INC. 078870292 manufacture(59735-565)
