Label: JACK BLACK SHAVE ESSENTIALS- avobenzone, octinoxate lotion
- NDC Code(s): 66738-541-40
- 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 Ingredient
- Purpose
- Use
- Warnings
- DO NOT USE
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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Directions
Apply liberally 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, regularly use sunscreen with a broad-spectrum SPF value of 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
Aqua (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
- Other Information
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INGREDIENTS AND APPEARANCE
JACK BLACK SHAVE ESSENTIALS
avobenzone, octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-541 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.2 g in 100 mL Inactive Ingredients Ingredient Name Strength HASLEA OSTREARIA (UNII: Y87200QHN9) MELISSA OFFICINALIS (UNII: YF70189L0N) ALCOHOL (UNII: 3K9958V90M) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERETH-26 (UNII: NNE56F2N14) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) LAVENDER OIL (UNII: ZBP1YXW0H8) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) PALMARIA PALMATA (UNII: 7832HOY4ZQ) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D) PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6) LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK) ROSEMARY OIL (UNII: 8LGU7VM393) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) PHENETHYL BENZOATE (UNII: 0C143929GK) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN (UNII: 9F8ET54T05) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POLYSORBATE 60 (UNII: CAL22UVI4M) CORN OIL (UNII: 8470G57WFM) BUDDLEJA DAVIDII LEAF (UNII: X380815D32) PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y) SODIUM HYDROXIDE (UNII: 55X04QC32I) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) APPLE (UNII: B423VGH5S9) GLYCERIN (UNII: PDC6A3C0OX) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-541-40 44 mL in 1 KIT; Type 1: Convenience Kit of Co-Package 09/17/2020 06/01/2024 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/17/2020 06/01/2024 Labeler - Jack Black L.L.C. (847024036) Establishment Name Address ID/FEI Business Operations Swiss American CDMO 080170933 manufacture(66738-541)
