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Medicated Fade Creme with Sunscreen

Medically reviewed by Drugs.com. Last updated on Oct 16, 2019.

Dosage form: cream
Ingredients: HYDROQUINONE 0.02g in 1g, OCTINOXATE 0.025g in 1g
Labeler: Bluefield Associates, Inc.
NDC Code: 16708-002

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medicated Fade Creme with Sunscreen

PRINCIPAL DISPLAY PANEL

Active Ingredient

Hydroquinone U.S.P. 2%

Purpose

Skin Lightener

Active Ingredient

Octinoxate 2.5%

Purpose

Sunscreen

Uses:
  • Lightens dark discolorations on the skin such as age spots, dark patches or freckles that may occur from medication, pregnancy or exposure to the elements.
  • Contains a sunscreen to help prevent darkening from reoccurring.

Warnings

For External use only. Avoid contact with eyes. Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor.

Do Not use on

children under 12 years of age unless directed by a doctor.

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a doctor before use.

Questions or Comments?

1-800-423-0306 or sales@bluefieldInc.com

Directions
  • Spread a thin layer into patches on face, hands, arms or body..
  • Use twice daily or as directed by a doctor and in 4-6 weeks the effect should be evident.
  • Not for use on children under 12 except on doctor's intructions.

Inactive Ingredients

Water (Aqua), White Petrolatum, Cetyl Alcohol, Isopropyl Palmitate, Stearic Acid, Propylene Glycol, Stearic Acid, Ammonium Lauryl Sulfate, Dimethicone, Diazolidinyl Urea, Methylparaben, Propylparaben, Glyceryl Stearate,Sodium Metabisulfite, Ascorbic Acid, BHA, Propul Gallate,Trisodium EDTA, Fragrance (Parfum).

MEDICATED FADE CREME WITH SUNSCREEN 
hydroquinone and octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16708-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE0.02 g  in 1 g
OCTINOXATE (OCTINOXATE) OCTINOXATE0.025 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ASCORBIC ACID 
PROPYL GALLATE 
WATER 
EDETATE TRISODIUM 
GLYCERYL MONOSTEARATE 
CETYL ALCOHOL 
ISOPROPYL PALMITATE 
STEARIC ACID 
AMMONIUM LAURYL SULFATE 
DIMETHICONE 
EDETATE DISODIUM 
SODIUM METABISULFITE 
BUTYLATED HYDROXYTOLUENE 
METHYLPARABEN 
PROPYLPARABEN 
DIAZOLIDINYL UREA 
Packaging
#Item CodePackage Description
1NDC:16708-002-011 JAR in 1 BOX
1113.5 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A10/26/2015
Labeler - Bluefield Associates, Inc. (626594667)
Establishment
NameAddressID/FEIOperations
Bluefield Associates, Inc.626594667manufacture(16708-002)

 
Bluefield Associates, Inc.