NOURIFUSION- avobenzone, octinoxate, octisalate lotion 
Herbalife International of America Inc.

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.

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NouriFusion Sunscreen Broad Spectrum SPF 15 Moisturizing Lotion Normal to Oily

Active Ingredients

Avobenzone (2%)

Octinoxate (7%)

Octisalate (3%)

Purpose

Sunscreen

Uses

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

Warnings

For external use only

Do not use on damaged or broken skin

Stop use and ask a doctor if rash occurs

When using this product keep out of eyes. Rinse with water to remove

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

Directions

  • Apply liberally 15 minutes before sun exposure
  • Use a water resistant sunscreen if swimming or sweating
  • Reapply at least every 2 hours
  • 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 value of 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), Nylon-12, C12-15 Alkyl Benzoate, Cetyl Phosphate, Isopropyl Isostearate, Cetearyl Alcohol, Dimehticone, Panthenol, Tocopheryl Acetate, sodium Ascorbate, Tocopherol, Retinol, Epilobium Angustifolium Flower/Leaf/Stem Extract, Chlorella Vulgaris Extract, Trifolium Pratense (Clover) Leaf Extract, Arnica Montana Flower Extract, Algae Extract, Yeast Extract, hydrolyzed Algin, Sea Water, Potassium Azeloyl Diglycinate, Allantoin, Butylene Glycol, Wheat Germ Glycerides, Dipropylene Glycol Dibenzoate, Caprylic/Capric Triglyceride, PPG-15 Stearyl Ether Benzoate, Ceteareth-20, C13-14 Isoparaffin, Laureth-7, Carbomer, Aminomethyl Propanol, Disodium EDTA, Polyacrylamide, Phenoxyethanol, Methylparaben, Ethylparaben, Propylaraben, Butylparaben, Isobutylparaben, Yellow 5 (CI 19140)

Distributed by:

Herbalife International of America, Inc.

800 W. Olympic Blvd. Suite 406

Los Angeles, CA 90015, USA

Herbalife International Luxembourg S.a R.L.

L-1610 Luxembourg

Imported and Distributed in Canada by:

Herbalife of Canada Ltd.

Imprte et distibue au Canada par:

Herbalife du Canada Ltee

Clagary, Alberta, Canada T2B 3P1

Made in USA with US and imported ingredients

Fabrique aux Etats-Unis avec des ingredients

americains et importes

2012 HERBALIFE

Principal Display Panel

HERBALIFE

nouriFusion

sunscreen

broad spectrum SPF 15

moisturizing lotion

with conditioning antioxidant

vitamins A, C and E

normal to oily

normale a grasse

ecran solaire

large spectre FPS 15

lotion hydratante

avec vitamines

antioxydantes

revitalisantes A, C et E

DIN No. 02259206


Box label

container label

NOURIFUSION 
avobenzone, octinoxate, octisalate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51785-515
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.079 g  in 50 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3.535 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE1.52 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
WATER (UNII: 059QF0KO0R)  
NYLON-12 (UNII: 446U8J075B)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CETYL PHOSPHATE (UNII: VT07D6X67O)  
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PANTHENOL (UNII: WV9CM0O67Z)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SODIUM ASCORBATE (UNII: S033EH8359)  
TOCOPHEROL (UNII: R0ZB2556P8)  
RETINOL (UNII: G2SH0XKK91)  
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)  
CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
TRIFOLIUM PRATENSE LEAF (UNII: 612YOZ36DG)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
YEAST (UNII: 3NY3SM6B8U)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)  
ALLANTOIN (UNII: 344S277G0Z)  
WHEAT GERM OIL (UNII: 14C97E680P)  
DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POLYACRYLAMIDE (CROSSLINKED; 0.01-0.2 MOLE PERCENT BISACRYLAMIDE) (UNII: RHA9LWJ494)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
NORI (UNII: 477TV3P5UX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51785-515-0150 mL in 1 TUBE; Type 0: Not a Combination Product09/25/201211/08/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35209/25/201211/08/2017
Labeler - Herbalife International of America Inc. (873035968)

Revised: 11/2017
 
Herbalife International of America Inc.