NADINOLA SKIN FADE FOR DRY SKIN- hydroquinone, octisalate cream

Nadinola Skin Fade for Dry Skin by

Drug Labeling and Warnings

Nadinola Skin Fade for Dry Skin by is a Otc medication manufactured, distributed, or labeled by J. Strickland & Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

NADINOLA SKIN FADE FOR DRY SKIN 
hydroquinone, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	20 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
CETYL ALCOHOL (UNII: 936JST6JCN)
PEG-100 STEARATE (UNII: YD01N1999R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM BISULFITE (UNII: TZX5469Z6I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-012-00	1 in 1 CARTON	06/01/1983
1		64 g in 1 JAR; Type 0: Not a Combination Product

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	Business Operations
J. Strickland & Co.		007023112	manufacture(12022-012) , pack(12022-012) , label(12022-012)