RODAN AND FIELDS UNBLEMISH- titanium dioxide, zinc oxide lotion 
Bentley Laboratories, LLC

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ACTIVE INGREDIENTS:

Titanium Dioxide 0.7%
Zinc Oxide 4.75%

PURPOSE:

Sunscreens

KEEP OUT OF REACH OF CHILDREN:

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

USES:

Helps prevent sunburn.

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 warm water to remove.

DIRECTIONS:

Apply a generous dime-sized amount evenly over the entire face every morning, 15 minutes before sun exposure, as the final step in the Regimen. Reapply every 2 hours when exposed to the sun. Avoid the eye area.

INACTIVE INGREDIENTS:

Water, Cyclopentasiloxane, Isododecane, Pentylene Glycol, Cetearyl Alcohol, Polysilicone-11, PEG-10 Dimethicone, Butylene Glycol, Polysorbate 60, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, PEG-100 Stearate, Glyceryl Stearate, Caprylyl Glycol, Squalane, Citric Acid, Xanthan Gum, 1,2-Hexanediol, PEG-60 Almond Glycerides, Ceteth-10 Phosphate, Oleanolic Acid, Nordihydroguaiaretic Acid, Glycerin, Carbomer, Chlorphenesin, Dimethiconol, Dicetyl Phosphate, Cholesterol, Hexyl Laurate, Fragrance, Polyglyceryl-4 Isostearate, Potassium Sorbate, Sodium Benzoate, Tocopherol, Disodium EDTA, Tetrahexyldecyl Ascorbate, Azelaic Acid, Stearic Acid, Lecithin, Alumina, Sodium Chondroitin Sulfate, Atelocollagen, Boerhavia Diffusa Root Extract, Methylisothiazolinone, Tropolone

RODAN and FIELDS UNBLEMISHED Label

RODAN and FIELDS UNBLEMISHED

4 Oil Control Lotion

BROAD SPECTRUM SPF 20 SUNSCREEN

Manufactured for Rodan and Fields, LLC
San Francisco, CA 94105
Made in USA  UNSS030  85-07-0015
Please recycle
visit rodanandfields.com

QUESTIONS OR COMMENTS
1-888-995-5656

30mL/1 Fl. Oz.

RF_Unblemished

RF_Unblemished1

RODAN AND FIELDS UNBLEMISH 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-122
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.21000 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1.42500 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
ISODODECANE (UNII: A8289P68Y2)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SQUALANE (UNII: GW89575KF9)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
XANTHAN GUM (UNII: TTV12P4NEE)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)  
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)  
OLEANOLIC ACID (UNII: 6SMK8R7TGJ)  
MASOPROCOL (UNII: 7BO8G1BYQU)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
TOCOPHEROL (UNII: R0ZB2556P8)  
EDETATE SODIUM (UNII: MP1J8420LU)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
AZELAIC ACID (UNII: F2VW3D43YT)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
TROPOLONE (UNII: 7L6DL16P1T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54111-122-5030 mL in 1 TUBE; Type 0: Not a Combination Product03/05/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02003/05/2010
Labeler - Bentley Laboratories, LLC (068351753)
Registrant - Bentley Laboratories, LLC (068351753)
Establishment
NameAddressID/FEIBusiness Operations
Bentley Laboratories, LLC068351753manufacture(54111-122)

Revised: 12/2023
Document Id: f2f0d967-ed98-4413-be5a-808313757c54
Set id: 2b3b6b62-364f-4aba-8024-3a73752b4c56
Version: 3
Effective Time: 20231219
 
Bentley Laboratories, LLC