Label: INFINITY- avobenzone, octinoxate, octisalate, octocrylene, oxybenzone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 54111-130-50 - Packager: Bentley Laboratories, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 December 19, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug FactsActive Ingredients
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
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Directions
For sunscreen use:
- Apply liberally 15 minutes before sun exposure
- Reapply at least every two hours
- Use a water resistant sunscreen if swimming or sweating
- For 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 a sunscreen with a Broad Spectrum SPF 15 or higher and other sun protection measures including:
- Limit time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeve shirts, pants, hats and sunglasses
- Other Information
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Inactive Ingredients
Water/Aqua/Eau, C12-15 Alkyl Benzoate, Glycerin, Cyclopentasiloxane, C14-22 Alcohols, Trisiloxane, Dimethicone, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Nymphaes Coerulea Flower Extract, Leuconostoc/Radish Root Ferment Filtrate, Rosmarinus Officinalis (Rosemary) Leaf Extract, Laminaria Digitata Extract, Zostera Marina Extract, Camellia Japonica Seed Oil, Sodium Carrageenan, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Acetyl Hexapeptide-8, Sea Salt/Maris Sal/Sel Marin, Diatomaceous Earth, Silica, C12-20 Alkyl Gluoside, Xanthan Gum, Ethylhexylglycerin, Glucose, Sodium Hydroxide, Phospholipids, Sorbital, Disodium EDTA, Potassium Sorbate, Citric Acid, Sodium Benzoate, Lecithin, Caprylyl Glycol, Butylene Glycol, Disodium EDTA, Magnesium Ascorbyl Phosphate, Sorbic Acid, Glyceryl Caprylate, Sodium Metabisulfite, Carbomer, Sodium Lactate, Polysorbate 20, Phenoxyethanol, Parfum?Fragrance, Linalool
- Questions? Comments?
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H2O BEAUTY INFINITY+ product label
H2O+™
BEAUTY
INFINITY+
WRINKLE DELAY CREAM
SPF30
AGE DEFYING PEPTIDES + SUN PROTECTION
50 mL 1.7 U.S. Fl oz
WATER
We plus it up with energy, confidence, and advanced technology. The result is positively smart.
H2O + INFINITY+ WINKLE DELAY CREAM
SPF 30PUMP THE BREAKS, WRINKLES l Put thise days of reckless sun-exposure behind you, leathery skin is so last year. The silky-texture of our Wrinkle Delay Cream with SPF 30 will quickly make you a believer. Featuring Camellia Japonica Oil and Red Algae extract, it protects against moisture loss and therefore helps ward off the appearance of wrinkles. Embrace the broad spectrum coverage and enjoy getting carded at the supermarket.
HOW TO USE
Massage on to face, neck, and chest every morning after cleansing and toning. Reapply every two hours. For best results, apply over your favorite H2O+ Beauty serum.H2O+
Distributed by: H2O Plus, LLC
San Francisco, CA 94104
WWW.H2OPLUS.COM
2016 MADE IN THE USA
083-50123-001 50123
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INGREDIENTS AND APPEARANCE
INFINITY
avobenzone, octinoxate, octisalate, octocrylene, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54111-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1.5 g in 50 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.75 g in 50 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.5 g in 50 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 2.5 g in 50 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.5 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) C14-22 ALCOHOLS (UNII: B1K89384RJ) DIMETHICONE (UNII: 92RU3N3Y1O) TRISILOXANE (UNII: 9G1ZW13R0G) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SUNFLOWER OIL (UNII: 3W1JG795YI) NYMPHAEA CAERULEA FLOWER (UNII: S9560USZ74) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) ROSEMARY (UNII: IJ67X351P9) LAMINARIA DIGITATA (UNII: 15E7C67EE8) ZOSTERA MARINA SEED (UNII: 2H467I6F58) CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T) CARRAGEENAN SODIUM (UNII: 7CY8BVL34N) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) SEA SALT (UNII: 87GE52P74G) DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85) CALCIUM ALUMINOSILICATE (UNII: 3L00JH8411) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) SODIUM HYDROXIDE (UNII: 55X04QC32I) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SORBITOL (UNII: 506T60A25R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETATE DISODIUM (UNII: 7FLD91C86K) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) SORBIC ACID (UNII: X045WJ989B) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) SODIUM METABISULFITE (UNII: 4VON5FNS3C) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) SODIUM LACTATE (UNII: TU7HW0W0QT) POLYSORBATE 20 (UNII: 7T1F30V5YH) PHENOXYETHANOL (UNII: HIE492ZZ3T) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54111-130-50 50 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 06/01/2016 Labeler - Bentley Laboratories, LLC (068351753)