Nadinola Skin Fade for Oily Skin

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

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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:12022-013
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (HYDROQUINONE)	HYDROQUINONE	20 mg in 1 g
OCTISALATE (OCTISALATE)	OCTISALATE	30 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER
GLYCERYL MONOSTEARATE
ISOPROPYL MYRISTATE
POLYETHYLENE GLYCOL 400
CETYL ALCOHOL
PEG-100 STEARATE
CITRIC ACID MONOHYDRATE
METHYLPARABEN
PROPYLPARABEN
SODIUM BISULFITE

Packaging
#	Item Code	Package Description
1	NDC:12022-013-00	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	06/01/1983

Labeler - J. Strickland & Co. (007023112)

Registrant - J. Strickland & Co. (007023112)

Establishment
Name	Address	ID/FEI	Operations
J. Strickland & Co.		007023112	manufacture(12022-013), pack(12022-013), label(12022-013)

Revised: 01/2018

Document Id: 6324462d-90a5-6012-e053-2991aa0a24de

Set id: dc915d8e-432e-42a9-8175-821faf795ac2

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