Natural Advantage AM SPF 15 All Day Moisture with AHAs

Jane Seymour Natural Advantage by

Drug Labeling and Warnings

Jane Seymour Natural Advantage by is a Otc medication manufactured, distributed, or labeled by Guthy-Renker LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

JANE SEYMOUR NATURAL ADVANTAGE  AM SPF 15 ALL DAY MOISTURE WITH AHAS- octinoxate, oxybenzone, and octisalate cream 
THE PROACTIV COMPANY LLC

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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Natural Advantage AM SPF 15 All Day Moisture with AHAs

SPL UNCLASSIFIED SECTION

Drug Facts

Directions

Apply to face every morning after cleansing.

WARNINGS

For external use only.

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, flush gently and thoroughly with water.

OTC - STOP USE SECTION

Discontinue use if rash or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Sun Alert

Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

Active Ingredients

Octinoxate 7.5%, Oxybenzone 4.0%, Octisalate 3.5%

Other Ingredients

Water (Aqua), Glycolic Acid, Glycerin, Ammonium Hydroxide, Steareth-20, Hexyl Laurate, Dimethicone, Steareth-2, Cetyl Alcohol, DEA-Cetyl Phosphate, PEG-100 Stearate, Methyl Methacrylate Crosspolymer, Camellia Oleifera Leaf Extract, Ormenis Multicaulis Oil, Tocopheryl Acetate, Allantoin, Panthenol, Butylene Glycol, Propylene Glycol, Glyceryl Stearate, Octyldodecyl Neopentanoate, Stearic Acid, Magnesium Aluminum Silicate, Xanthan Gum, Disodium EDTA, Diazolidinyl Urea, Methylparaben, Propylparaben, Aluminum Hydroxide, (CI 77002), Titanium Dioxide (CI 77891)

PRINCIPAL DISPLAY PANEL - 30 ml Tube

NATURAL
ADVANTAGE®

By
Jane Seymour

All Day Moisture
With SPF 15

1 fl oz 30 ml e

Principal Display Panel – 30 ml Tube

PRINCIPAL DISPLAY PANEL - 50 ml Tube

NATURAL
ADVANTAGE®

By
Jane Seymour

All Day Moisture
With SPF 15

2 fl oz 50 ml e

Principal Display Panel – 50 ml Tube
JANE SEYMOUR NATURAL ADVANTAGE   AM SPF 15 ALL DAY MOISTURE WITH AHAS
octinoxate, oxybenzone, and octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 11410-150
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate0.075 g  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone0.04 g  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate0.035 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11410-150-1130 mL in 1 TUBE; Type 0: Not a Combination Product04/26/200501/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35204/26/200501/01/2019
JANE SEYMOUR NATURAL ADVANTAGE   AM SPF 15 ALL DAY MOISTURE WITH AHAS
octinoxate, oxybenzone, and octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 11410-160
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate0.075 g  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone0.04 g  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate0.035 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11410-160-2250 mL in 1 TUBE; Type 0: Not a Combination Product04/26/200501/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35204/26/200501/01/2019
Labeler - THE PROACTIV COMPANY LLC (080216357)
Registrant - THE PROACTIV COMPANY LLC (080216357)

Revised: 1/2020
 
THE PROACTIV COMPANY LLC