Label: AMBI EVEN AND CLEAR FACIAL MOISTURIZER SPF-30- avobenzone, octisalate, octocrylene cream
- NDC Code(s): 73453-233-00
- Packager: AMBI Enterprises LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 19, 2024
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- Drug Facts:
- Active ingredients:
- Uses:
- Warnings:
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Directions:
- Apply liberally 15-minutes before sun exposure.
- Reapply:
- At least every two-hours.
- Immediately after swimming, sweating or towel drying.
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection and other sun measures including: SUN PROTECTION MEASURES:
- Limit time in the sun, especially between 10 am and 2 pm.
- Wear long sleeve shirts, pants, hats and sunglasses.
- For children under 6-months, consult a physician.
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Inactive ingredients:
Acrylates Copolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arctostaphylos Uva Ursi (Bearberry) Leaf Extract, Ascorbyl Palmitate (Vitamin C), Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetearyl Glucoside, Cetyl Alcohol, Cucumis Sativa (Cucumber) Extract, Cyclopentasiloxane, Cyclotetrasiloxane, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extarct, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Magnesium Aluminum Silicate, Phenoxyethanol, Polysorbate 20, Saccharide Isomerate, Silica, Sodium Hydroxide, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E).
- Other information:
- Questions or comments?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
AMBI EVEN AND CLEAR FACIAL MOISTURIZER SPF-30
avobenzone, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73453-233 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) ASCORBYL PALMITATE (UNII: QN83US2B0N) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETYL ALCOHOL (UNII: 936JST6JCN) CUCUMBER (UNII: YY7C30VXJT) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LICORICE (UNII: 61ZBX54883) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYALURONIC ACID (UNII: S270N0TRQY) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SACCHARIDE ISOMERATE (UNII: W8K377W98I) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73453-233-00 1 in 1 BOX 09/25/2021 1 50 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 09/25/2021 Labeler - AMBI Enterprises LLC (117015229)
