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Othine Skin Bleach

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

Dosage form: cream
Ingredients: HYDROQUINONE 30mg in 1g, OCTISALATE 30mg in 1g
Labeler: J. Strickland & Co.
NDC Code: 12022-016

Othine Skin Bleach Cream

Active Ingredients

Hydroquinone, 3%; 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 broken skin 
  • to prevent sunburn 
  • if product is tan or brown.

When using this product,
  • mild irritation 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 consukt a doctor if
  • a gradual blue-black darkening of the skin occurs 
  • irritation becomes 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

consult a health professional before use.

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 to affected area twice daily, or as directed by a doctor.
  • If going outside, use a sunscreen or wear protective clothing
  • Children under 12 years of age, ask a doctor before use.

Inactive Ingredients:

water, mineral oil, stearyl alcohol, decyl oleate, glyceryl stearate, oleth-20, laureth-23, propylene glycol, stearamidopropyl dimethylamine, citric acid, sodium metabisulfite, methylparaben, propylparaben, fragrance

Package Labeling

OTHINE SKIN BLEACH 
hydroquinone, octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-016
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE30 mg  in 1 g
OCTISALATE (OCTISALATE) OCTISALATE30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER 
MINERAL OIL 
STEARYL ALCOHOL 
DECYL OLEATE 
GLYCERYL MONOSTEARATE 
OLETH-20 
LAURETH-23 
PROPYLENE GLYCOL 
STEARAMIDOPROPYL DIMETHYLAMINE 
CITRIC ACID MONOHYDRATE 
SODIUM METABISULFITE 
METHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:12022-016-001 JAR in 1 CARTON
164 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A07/01/1974
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIOperations
J. Strickland & Co.007023112manufacture(12022-016), pack(12022-016), label(12022-016)

 
J. Strickland & Co.

Further information

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