Natural Advantage SPF 15 All Day Moisture with AHA

Natural Advantage SPF 15 All Day Moisture with AHAs by

Drug Labeling and Warnings

Natural Advantage SPF 15 All Day Moisture with AHAs by is a Otc medication manufactured, distributed, or labeled by Guthy-Renker LLC, AMCOL Health & Beauty Solutions, Incorporated, Thibiant International, Inc., Procore Laboratories, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATURAL ADVANTAGE SPF 15 ALL DAY MOISTURE WITH AHAS - octinoxate, oxybenzone, 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 SPF 15 All Day Moisture with AHA

DIRECTIONS:

Apply to face every morning after cleansing.

WARNINGS:

For external use only. Avoid contact with eyes. If eye contact occurs, flush gently and thoroughly with water. 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, Glycolic Acid, Glycerin, Steareth-20, PEG-100 Stearate, Hexyl Laurate, Dimethicone, Steareth-2, Cetyl Alcohol, DEA-Cetyl Phosphate, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Ammonium Hydroxide, Camellia Oleifera Leaf Extract, Ormenis Multicaulis Oil, Tocopheryl Acetate, Allantoin, Panthenol, Butylene Glycol, Propylene Glycol, Glyceryl Stearate, Octyldodecyl Neopentanoate, Stearic Acid, Bentonite, Xanthan Gum, Octyldodecanol, Disodium EDTA, Diazolidinyl Urea, Methyparaben, Propylparaben, Aluminum Hydroxide, Titanium Dioxide

Made in the USA of foreign and
domestic components

Distributed by: Guthy-Renker ®, LLC
P.O. Box 14383
Palm Desert, CA 92255-4383
London UK SW1Y 4HH, Sydney, Australia 2138
Auckland, New Zealand, Toronto, Ontario M1X 1E7

Principal Display Panel – 25 mL Tube

Natural Advantage®

Jane Seymour

AM

SPF 15

All Day Moisture

With AHAs

0.85 fl oz 25 mL e

Principal Display Panel – 50 mL Tube

Natural Advantage®

Jane Seymour

AM

SPF 15

All Day Moisture

With AHAs

1.7 fl oz 50 mL e

NATURAL ADVANTAGE SPF 15 ALL DAY MOISTURE WITH AHAS 
octinoxate, oxybenzone, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11410-413
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	7.5 g  in 100 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	4 g  in 100 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	3.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCOLIC ACID (UNII: 0WT12SX38S)
GLYCERIN (UNII: PDC6A3C0OX)
STEARETH-20 (UNII: L0Q8IK9E08)
PEG-100 STEARATE (UNII: YD01N1999R)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
DIMETHICONE (UNII: 92RU3N3Y1O)
STEARETH-2 (UNII: V56DFE46J5)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
AMMONIA (UNII: 5138Q19F1X)
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
CLADANTHUS MIXTUS FLOWER VOLATILE OIL (UNII: RAY2FRM711)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
ALLANTOIN (UNII: 344S277G0Z)
PANTHENOL (UNII: WV9CM0O67Z)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
STEARIC ACID (UNII: 4ELV7Z65AP)
BENTONITE (UNII: A3N5ZCN45C)
XANTHAN GUM (UNII: TTV12P4NEE)
OCTYLDODECANOL (UNII: 461N1O614Y)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11410-413-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	11/02/2009	01/01/2019
2	NDC: 11410-413-02	25 mL in 1 TUBE; Type 0: Not a Combination Product	11/02/2009	01/01/2019
3	NDC: 11410-413-03	50 mL in 1 TUBE; Type 0: Not a Combination Product	11/02/2009	01/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/02/2009	01/01/2019

Labeler - THE PROACTIV COMPANY LLC (080216357)

Registrant - THE PROACTIV COMPANY LLC (080216357)

Revised: 1/2020

Document Id: 7c6c8e9e-bb9c-47f3-a33e-521bb68b26c8

34390-5

Set id: 6c801471-947a-4783-9742-ed9add888a18

Version: 3

Effective Time: 20200114

 

THE PROACTIV COMPANY LLC