Othine Skin Bleach

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

Medically reviewed by Drugs.com. Last updated on Jan 9, 2024.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:12022-016
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (HYDROQUINONE)	HYDROQUINONE	30 mg in 1 g
OCTISALATE (OCTISALATE)	OCTISALATE	30 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description
1	NDC:12022-016-00	1 JAR in 1 CARTON
1		64 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358A	07/01/1974

Labeler - J. Strickland & Co. (007023112)

Registrant - J. Strickland & Co. (007023112)

Establishment
Name	Address	ID/FEI	Operations
J. Strickland & Co.		007023112	manufacture(12022-016), pack(12022-016), label(12022-016)

Document Id: 6324462d-90c6-6012-e053-2991aa0a24de

Set id: 03e2bbac-f31a-407f-aa3e-639851c6c00a

Version: 1

Effective Time: 20180119

J. Strickland & Co.

Further information

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

Medical Disclaimer

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