Label: DOUBLE-DUTY FACE MOISTURIZER- mositurizing sunscreen lotion
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NDC Code(s):
66738-020-01,
66738-020-02,
66738-020-03,
66738-020-04, view more66738-020-16, 66738-020-19, 66738-020-50
- Packager: Jack Black, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 7, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
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Inactive Ingredients
Purified Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenylethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate / Sodium Acryloyl Dimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavendula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens (Geranium) Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis (Balm Mint) Extract, Haslea Ostreaia (Blue Algae) Extract, Palmaria Palmata (Sea Parsley) Extract, Calendula Officinalis (Calendula) Flower Extract, Glycerin, Leontopodium Alöinum (Edelweiss) Extract, Artemisia Umbelliformis Extract, Buddleja Davidii Leaf Extract, Peucedanum Ostruthium Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Anthemis Nobilis (Roman Chamomile) Flower Oil
- Use
- Use
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- Use a water resisitant sunscreen if swimming or sweating
- Reapply at least every two 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, use sunscreen with a broad spectrum SPF15 or higher
- Limit time in the sun, especxially from 10 a.m. - 2 p.m.
- Wear long sleeve shirts, pants, hats and sunglasses.
- KEEP OUT OF REACH OF CHILDREN
- Other Information
- Questions?
- Labeling
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INGREDIENTS AND APPEARANCE
DOUBLE-DUTY FACE MOISTURIZER
mositurizing sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.2 g in 1000 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 1000 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) PHENETHYL BENZOATE (UNII: 0C143929GK) HASLEA OSTREARIA (UNII: Y87200QHN9) HYALURONATE SODIUM (UNII: YSE9PPT4TH) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) GLYCERIN (UNII: PDC6A3C0OX) LAVENDER OIL (UNII: ZBP1YXW0H8) ROSEMARY OIL (UNII: 8LGU7VM393) MELISSA OFFICINALIS LEAF OIL (UNII: PTP6R7263M) PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y) BUDDLEJA DAVIDII LEAF (UNII: X380815D32) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERETH-26 (UNII: NNE56F2N14) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CARBOMER 934 (UNII: Z135WT9208) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM (UNII: 7FLD91C86K) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) DULSE (UNII: 7832HOY4ZQ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWER (UNII: MWN6IZU3XM) APPLE FRUIT OIL (UNII: 9NT987I3A8) ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC) Product Characteristics Color white (Opaque Lotion) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-020-03 97 g in 1 BOTTLE; Type 0: Not a Combination Product 05/29/2009 2 NDC:66738-020-04 44 g in 1 TUBE; Type 0: Not a Combination Product 07/30/2009 3 NDC:66738-020-19 251 g in 1 BOTTLE; Type 0: Not a Combination Product 06/15/2011 4 NDC:66738-020-01 30 g in 1 TUBE; Type 0: Not a Combination Product 04/01/2020 5 NDC:66738-020-16 480 g in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 6 NDC:66738-020-50 14 g in 1 TUBE; Type 0: Not a Combination Product 03/11/2020 7 NDC:66738-020-02 2 g in 1 PACKET; Type 0: Not a Combination Product 03/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/29/2009 Labeler - Jack Black, LLC (847024036)