Label: TOUCH ANTI-AGING SPF 30 MOISTURIZER- zinc oxide, octinoxate, and octisalate cream
- NDC Code(s): 73246-002-01
- Packager: Diractions Capital LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 13, 2023
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS
- PURPOSE
- Uses
- Warnings
- Directions
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Inactive Ingredients
Aqua, C12-15 Alkyl Benzoate, Glyceryl Stearate, Cetyl Alcohol, Cetearyl Ethylhexanoate, Cyclopentasiloxane, Cetearyl Alcohol, Cetyl Dimethocone, Ascorbic Acid, Tocopherol Acetate, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ginkgo Biloba Leaf Extract, PEG-100 Stearate, Panax Ginseng Root Extract, Camellia Oleifera Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Sodium PCA, Sodium Hyaluronate, Xanthan Gum, Dehydroacetic Acid, Triethoxycaprylylsilane, Benzyl Alcohol, Tetrasodium EDTA, Citric Acid.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label
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INGREDIENTS AND APPEARANCE
TOUCH ANTI-AGING SPF 30 MOISTURIZER
zinc oxide, octinoxate, and octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73246-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 70 mg in 1 mL Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 75 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETYL ALCOHOL (UNII: 936JST6JCN) CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL DIMETHICONE 45 (UNII: IK315POC44) ASCORBIC ACID (UNII: PQ6CK8PD0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02) GINKGO BILOBA WHOLE (UNII: 660486U6OI) PEG-100 STEARATE (UNII: YD01N1999R) PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) HYALURONATE SODIUM (UNII: YSE9PPT4TH) XANTHAN GUM (UNII: TTV12P4NEE) DEHYDROACETIC ACID (UNII: 2KAG279R6R) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE SODIUM (UNII: MP1J8420LU) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73246-002-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 03/04/2020 Labeler - Diractions Capital LLC (117719327)