Label: JACK BLACK THE SUPREME SHAVE- avobenzone, octinoxate lotion
- NDC Code(s): 66738-631-40
- Packager: Jack Black L.L.C
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 23, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Use
- Warnings
- DO NOT USE
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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Directions
Apply liberally after cleansing and shaving and 15 minutes before sun exposure. • Use a water-resistant 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 SPF 15 or higher. • Limit time in the sun, especially from 10 a.m. – 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses.
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Inactive Ingredients
Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavandula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis Extract, Haslea Ostrearia Extract, Palmaria Palmata Extract, Calendula Officinalis Flower Extract*, Glycerin, Leontopodium Alpinum (Edelweiss) Extract*, Retinyl Palmitate, Tocopheryl Acetate, Anthemis Nobilis Flower Oil, Peucedanum Ostruthium Leaf Extract*, Buddleja Davidii Leaf Extract*, Artemisia Umbelliformis Extract*.
* Certified Organic
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INGREDIENTS AND APPEARANCE
JACK BLACK THE SUPREME SHAVE
avobenzone, octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-631 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 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) HYALURONATE SODIUM (UNII: YSE9PPT4TH) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) PALMARIA PALMATA (UNII: 7832HOY4ZQ) GLYCERIN (UNII: PDC6A3C0OX) APPLE (UNII: B423VGH5S9) ROSEMARY OIL (UNII: 8LGU7VM393) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) MELISSA OFFICINALIS (UNII: YF70189L0N) CORN OIL (UNII: 8470G57WFM) HASLEA OSTREARIA (UNII: Y87200QHN9) PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6) LAVENDER OIL (UNII: ZBP1YXW0H8) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y) BUDDLEJA DAVIDII LEAF (UNII: X380815D32) POLYSORBATE 60 (UNII: CAL22UVI4M) SODIUM HYDROXIDE (UNII: 55X04QC32I) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PHENETHYL BENZOATE (UNII: 0C143929GK) GLYCERETH-26 (UNII: NNE56F2N14) HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN (UNII: 9F8ET54T05) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-631-40 44 mL in 1 KIT; Type 1: Convenience Kit of Co-Package 07/29/2021 06/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/30/2020 06/01/2024 Labeler - Jack Black L.L.C (847024036) Establishment Name Address ID/FEI Business Operations Swiss American CDMO 080170933 manufacture(66738-631)