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Nadinola Skin Fade for Oily Skin

Medically reviewed by Drugs.com. Last updated on Jan 11, 2021.

Dosage form: cream
Ingredients: HYDROQUINONE 20mg in 1g, OCTISALATE 30mg in 1g
Labeler: J. Strickland & Co.
NDC Code: 12022-013

Nadinola Skin Fade Cream for Oily Skin

Active Ingredients:

Hydroquinone, 2%, Octisalate, 3%

Purpose

Skin Lightener

Sunscreen

Uses:

Gradually fades areas of skin discoloration such as

  • age spots 
  • freckles 
  • liver spots 
  • dark areas that can occur while using oral contraceptives.

Warnings:

For External Use Only.

Do not use
  • on inflamed or brocken skin 
  • to prevent sunburn  
  • if product is tan or brown

When using this product
  • mild irration may occur 
  • avoid contact with eyes. If contact occurs, Rinse With water.
  • avoid unnecessary sun exposure and use a sunscreen or protective clothing

Stop use and ask a doctor if
  • a gradual blue black darkening of the skin occurs 
  • irritation is severe 
  • no improvement is seen after 3 months

If pregnant or breast-feeding

consult a health professional before use

Keep out of reach of children

Directions:
  • If skin is sensitive, test on a small area inside elbow overnight before use. 
  • Adults and children 12 years and older, apply as a thin layer toaffected area twice daily, or as directed by a doctor.
  • If going outside, use a sunscreen or wear protective clothong. 
  • Children under 12 years of age, ask a doctor before use.

Inactive Ingredients:

water, glyceryl stearate, isopropyl myristate, PEG-8, cetyl alcohol, PEG-100 stearate, fragrance, citric acid, methylparaben, propylparaben, sodium bisulfite.

Package Labeling

NADINOLA SKIN FADE FOR OILY SKIN 
hydroquinone, octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-013
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE20 mg  in 1 g
OCTISALATE (OCTISALATE) OCTISALATE30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERYL MONOSTEARATE 
ISOPROPYL MYRISTATE 
POLYETHYLENE GLYCOL 400 
CETYL ALCOHOL 
PEG-100 STEARATE 
CITRIC ACID MONOHYDRATE 
METHYLPARABEN 
PROPYLPARABEN 
SODIUM BISULFITE 
Packaging
#Item CodePackage Description
1NDC:12022-013-001 JAR in 1 CARTON
164 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A06/01/1983
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIOperations
J. Strickland & Co.007023112manufacture(12022-013), pack(12022-013), label(12022-013)

 
J. Strickland & Co.

Further information

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