Label: WEIGHTLESS PROTECTION SPF 30- octinoxate, zinc oxide, octisalate lotion
- NDC Code(s): 70712-102-11
- Packager: Botanical Science Technologies
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 9, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
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WARNINGS
FOR EXTERNAL USE ONLY. DO NOT USE ON DAMAGED OR BROKEN SKIN. WHEN USING THIS PRODUCT, KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE. STOP USE AND CONSULT WITH A PHYSICIAN IF RASH OCCURS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY. SUN ALERT: LIMITING SUN EXPOSURE AND USING SUNSCREENS MAY REDUCE THE RISKS OF SKIN AGING, SKIN CANCER, AND OTHER HARMFUL EFFECTS OF THE SUN.
- DIRECTIONS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENTS
PURIFIED WATER, GLYCERYL STEARATE, PEG-100 STEARATE, C12-15 ALKYL BENZOATE, HYDROGENATED VEGETABLE OIL, CETYL ALCOHOL, CETEARETH-20, CYCLOMETHICONE, CETYL DIMETHICONE COPOLYOL, CETYL DIMETHICONE, ASCORBIC ACID (VIT C), RETINYL PALMITATE, TOCOPHERYL ACETATE (VIT E), CAMELLIA OLEIFERA (JAPANESE GREEN TEA) EXTRACT, CHAMOMILE (ANTHEMIS NOBOLIS) EXTRACT, CALENDULA OFFICINALIS EXTRACT, GINSENG (PANAX GINSENG) EXTRACT, GINGKO BILOBA EXTRACT, LICORICE (GLYCYRRHIZA GLABRA) EXTRACT, SODIUM HYALURONATE, SODIUM PCA, CITRIC ACID, METHYLPARABEN, XANTHAN GUM, TETRASODIUM EDTA, DIAZOLIDINYL UREA
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
WEIGHTLESS PROTECTION SPF 30
octinoxate, zinc oxide, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70712-102 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 7 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETYL ALCOHOL (UNII: 936JST6JCN) HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CYCLOMETHICONE (UNII: NMQ347994Z) CETYL DIMETHICONE 45 (UNII: IK315POC44) ASCORBIC ACID (UNII: PQ6CK8PD0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CALENDULA OFFICINALIS WHOLE (UNII: PFR03EBU0H) CHAMAEMELUM NOBILE WHOLE (UNII: 7NF3GE7IWR) GINKGO BILOBA WHOLE (UNII: 660486U6OI) PEG-100 STEARATE (UNII: YD01N1999R) PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) HYALURONATE SODIUM (UNII: YSE9PPT4TH) XANTHAN GUM (UNII: TTV12P4NEE) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) METHYLPARABEN (UNII: A2I8C7HI9T) EDETATE SODIUM (UNII: MP1J8420LU) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70712-102-11 87 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/09/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/09/2022 Labeler - Botanical Science Technologies (783654275)
