PRINCIPAL SECRET RECLAIM SUNSCREEN FOR FACE AND BODY SPF 30- meradimate, octinoxate, oxybenzone, and zinc oxide cream 
Guthy-Renker LLC

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Principal Secret® Reclaim® Sunscreen For Face & Body SPF 30

Drug Fact Label

Active ingredient

Octinoxate 7.5%
Meradimate 3.5%
Zinc Oxide 2.0%
Oxybenzone 2.0%

Purpose

Sunscreen

Uses

Warnings

Skin Cancer/Skin Aging Alert

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

For external use only.

Do not use

on damaged or broken skin.

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

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water, Ethylhexyl Ethylhexanoate, Pentylene Glycol, Triisononanoin, Sodium Dihydroxycetyl Phosphate, Glyceryl Stearate SE, Cetearyl Alcohol, Beeswax, Glycosaminoglycans, Ahnfeltiopsis Concinna Extract, Acetyl Hexapeptide-8, Phospholipids, Tocopheryl Acetate, Retinyl Palmitate, Cucumis Melo (Melon) Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Ascorbyl Palmitate, Pantothenic Acid, Vitis Vinifera (Grape) Leaf Extract, Iris Florentina Root Extract, Hibiscus Abelmoschus Extract, Bisabolol, Hydrogenated Palm Glycerides, Ceteareth-20, Polyglyceryl-3 Caprate, Phytonadione, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Xanthan Gum, Caprylic/Capric Triglyceride, Butylene Glycol, Phenoxyethanol, Methylparaben, Chlorphenesin, Benzoic Acid

Other Information

Questions or comments?

800-510-4961

Dist. by: Guthy-Renker® LLC • PO Box 14383 • Palm Desert,
CA 92255-4383

PRINCIPAL DISPLAY PANEL - 75 mL Tube Label

PRINCIPAL
SECRET®

RECLAIM®
with Argireline®

Sunscreen
For Face & Body
SPF 30

75 mL 2.5 FL. OZ.

PRINCIPAL DISPLAY PANEL - 75 mL Tube Label
PRINCIPAL SECRET RECLAIM SUNSCREEN FOR FACE AND BODY SPF 30 
meradimate, octinoxate, oxybenzone, and zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70605-014
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Meradimate (UNII: J9QGD60OUZ) (Meradimate - UNII:J9QGD60OUZ) Meradimate3.5 mg  in 100 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate7.5 mg  in 100 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone2 mg  in 100 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide3 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Ethylhexyl Ethylhexanoate (UNII: 430RJA6715)  
Pentylene Glycol (UNII: 50C1307PZG)  
Triisononanoin (UNII: XF4K22WN6T)  
Sodium Dihydroxycetyl Phosphate (UNII: YWI33EV595)  
Glyceryl Stearate SE (UNII: FCZ5MH785I)  
Cetostearyl Alcohol (UNII: 2DMT128M1S)  
Yellow Wax (UNII: 2ZA36H0S2V)  
Ahnfeltiopsis Concinna (UNII: SMF2K46G8D)  
Acetyl Hexapeptide-8 (UNII: L4EL31FWIL)  
Lecithin, Soybean (UNII: 1DI56QDM62)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
MUSKMELON (UNII: ZV095H5633)  
BANANA (UNII: 4AJZ4765R9)  
Ascorbyl Palmitate (UNII: QN83US2B0N)  
Pantothenic Acid (UNII: 19F5HK2737)  
VITIS VINIFERA LEAF (UNII: R1H893D80E)  
IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT (UNII: M30XO5X4XD)  
ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)  
LEVOMENOL (UNII: 24WE03BX2T)  
Hydrogenated Palm Glycerides (UNII: YCZ8EM144Q)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
Phytonadione (UNII: A034SE7857)  
Polyacrylamide (10000 MW) (UNII: E2KR9C9V2I)  
C13-14 Isoparaffin (UNII: E4F12ROE70)  
Laureth-7 (UNII: Z95S6G8201)  
Xanthan Gum (UNII: TTV12P4NEE)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Methylparaben (UNII: A2I8C7HI9T)  
Chlorphenesin (UNII: I670DAL4SZ)  
Benzoic Acid (UNII: 8SKN0B0MIM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70605-014-2175 mL in 1 TUBE; Type 0: Not a Combination Product11/30/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM02004/30/2016
Labeler - Guthy-Renker LLC (948861877)

Revised: 1/2024
Document Id: f61f0753-6794-4f18-8b4e-60ff19ec0334
Set id: 4a183aa2-deda-4b26-a126-6f98cfbdb0f3
Version: 3
Effective Time: 20240110
 
Guthy-Renker LLC