REN CLEAN FAVOURITES- zinc oxide 
REN Ltd

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REN Clean Favourites Kit

Drug Facts

Active ingredients

Zinc Oxide 22%

Purpose

Sunscreen

Uses

Warnings

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 swallowed, get medical help or contact Poison Control Center right away.

Directions

Other information 

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

Inactive ingredients

Aqua (Water), Caprylic/Capric Triglyceride, Aloe Barbadensis Leaf Juice, Glycerin, Caprylyl Caprylate/Caprate, Propanediol, Arachidyl Alcohol, Cetearyl Alcohol, Coco-Glucoside, Oryza Sativa Starch, Pongamia Glabra Seed Oil, Microcrystalline Cellulose, Behenyl Alcohol, Phenoxyethanol, Arachidyl Glucoside, Isostearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Polyhydroxystearic Acid, Passiflora Edulis Fruit Extract, Ethylhexylglycerin, Glyceryl Oleate, Vaccinium Macrocarpon (Cranberry) Seed Oil, Xanthan Gum, Cellulose Gum, Sodium Chloride, HippophaeRhamnoides Oil, Citrus Nobilis (Mandarin Orange) Peel Oil, Anthemis Nobilis Flower Oil, Cinnamomum Camphora Linalloliferum Wood Oil, Pelargonium Graveolens Flower Oil, Glucose, Parfum* (Fragrance), Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Rosmarinus Officinalis (Rosmary) Leaf Extract, Hydrogenated Palm Glycerides Citrate, Citric Acid, Sodium Hydroxide, Citronellol, Geraniol, Limonene, Linalool

*100% Natural Fragrance - Parfum 100% Naturel

Questions or comments?

please contact 800-437-3488 from 8:30-17:30 EST

Package Labeling: 51417-0003-1

Kit

Package Labeling: 51417-0002-5

BoxInner Package.

REN CLEAN FAVOURITES 
zinc oxide kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51417-0003
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51417-0003-11 in 1 KIT09/01/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 10 mL
Part 1 of 1
CLEAN SCREEN MINERAL SPF30 MATTIFYING FACE SUNSCREEN BROAD SPECTRUM 
zinc oxide cream
Product Information
Item Code (Source)NDC:51417-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION220 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)  
PROPANEDIOL (UNII: 5965N8W85T)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
COCO GLUCOSIDE (UNII: ICS790225B)  
STARCH, RICE (UNII: 4DGK8B7I3S)  
KARUM SEED OIL (UNII: 62160PU6FJ)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
DOCOSANOL (UNII: 9G1OE216XY)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL OLEATE (UNII: 4PC054V79P)  
CRANBERRY SEED OIL (UNII: 73KDS3BW5E)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MANDARIN OIL (UNII: NJO720F72R)  
CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)  
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
TOCOPHEROL (UNII: R0ZB2556P8)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51417-0002-11 in 1 BOX
110 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/01/2019
Labeler - REN Ltd (385613831)

Revised: 11/2023
Document Id: 0b58f5d5-37ca-da6e-e063-6394a90a804c
Set id: 252c3860-9204-4047-b990-71f21db42830
Version: 4
Effective Time: 20231130
 
REN Ltd