INFINITY- avobenzone, octinoxate, octisalate, octocrylene, oxybenzone cream

INFINITY by

Drug Labeling and Warnings

INFINITY by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive Ingredients

Avobenzone 3.0%

Octinoxare 7.5%

Octisalate 5.0%

Octocrylene 9.0%

Oxybenzone 5.0%

Purpose

Sunscreen

Keep out of reach of children

• Keep out of reach of children.
• If swallowed, get medical help or contact a Poison Control Center immediately.

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

avoid contact with eyes. If contact occurs, flush thoroughly with water

Stop use and ask a doctor

if rash occursf rash occurs

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

• Protect the product in this container from excessive heat and direct sun

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?

Call 1-800-242-2284, M - F 9am - 5PM PST

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 30

PUMP 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

INGREDIENTS AND APPEARANCE

INFINITY 
avobenzone, octinoxate, octisalate, octocrylene, oxybenzone cream

Product 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)