Label: LUXURY BODY RITUAL HYDRATING SPF 30- zinc oxide lotion
- NDC Code(s): 82404-102-11, 82404-102-12
- Packager: JANE STREET LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
-
DIRECTIONS
- APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
- CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR.
- USE A WATER-RESISTANT SUNSCREEN IF SWIMMING OR SWEATING.
- REAPPLY AT LEAST EVERY 2 HOURS.
- SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY 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 A.M. - 2 P.M.
- WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES.
- OTHER INFORMATION
-
INACTIVE INGREDIENTS
Water, Caprylic/Capric Triglyceride, Dimethicone, Butylene Glycol, Sodium Olivate, Silica, Cetearyl Alcohol, Cetearyl Olivate, Sorbitan Olivate, Caprylyl Glycol, Nymphaea Coerulea (Blue Lotus) Flower Extract, Orchis Maculata (Spotted Orchid) Flower Extract, Passiflora Edulis (Passion Fruit) Extract, Camellia Sinensis (Green Tea) Leaf Oil, Potassium Cetyl Phosphate, Stearic Acid, Xylitylglucoside, Anhydroxylitol, Cetearyl Glucoside, Triethoxycaprylylsilane, Xylitol, Tocopheryl Acetate, Xanthan Gum, Caprylhydroxamic Acid, Glycerin, Citric Acid, Pongamia Pinnata Seed Extract
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LUXURY BODY RITUAL HYDRATING SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82404-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 11 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM OLIVATE (UNII: ND5Y5M6ZUT) DACTYLORHIZA MACULATA FLOWER (UNII: G1H83709QF) DIMETHICONE (UNII: 92RU3N3Y1O) NYMPHAEA CAERULEA FLOWER (UNII: S9560USZ74) SORBITAN OLIVATE (UNII: MDL271E3GR) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) XANTHAN GUM (UNII: TTV12P4NEE) GREEN TEA LEAF (UNII: W2ZU1RY8B0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) STEARIC ACID (UNII: 4ELV7Z65AP) XYLITOL (UNII: VCQ006KQ1E) XYLITYLGLUCOSIDE (UNII: O0IEZ166FB) ANHYDROXYLITOL (UNII: 8XWR7NN42F) PASSIFLORA EDULIS FRUIT (UNII: 602YE42W5R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82404-102-12 1 in 1 BOX 05/01/2024 1 NDC:82404-102-11 120 mL 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 05/01/2024 Labeler - JANE STREET LLC (081575951)