ARTRA SKIN TONE FOR OILY SKIN- hydroquinone, homosalate, oxybenzone cream

Artra Skin Tone for Oily Skin by

Drug Labeling and Warnings

Artra Skin Tone for Oily 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, 7.5%

Homosalate, 2%

Oxybenzone, 2.5%

Purpose

Sunscreen

Skin Lightener

Sunscreen

Uses:

Gradually fades skin discolorations such as

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

Warnings:

For external use only

Do not use

• to prevent sunburn
• if product is tan or brown
• on inflamed or broken skin

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 consult a doctor if 

• a gradual blue-black darking 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

In case of accidental ingestion, get medical help or contact a poison control center.

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.
• Children under 12 years of age: ask a doctor before use.

Inactive Ingredients

water, glyceryl stearate, myristyl myristate, PEG-100 stearate, magnesium aluminum silicate, cetyl alcohol, dimenthicone, xanthan gum, stearic acid, palmitic acid, sodium sulfite, sodium lauryl sulfate, fragrance, citric acid, carathamus tinctorius (safflower) seed oil, ascorbic acid, methylparaben, tocopheryl acetate, aloe barbadensis leaf extract.

Package Labeling

INGREDIENTS AND APPEARANCE

ARTRA SKIN TONE FOR OILY SKIN 
hydroquinone, homosalate, oxybenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	75 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	20 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	25 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
PEG-100 STEARATE (UNII: YD01N1999R)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
XANTHAN GUM (UNII: TTV12P4NEE)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
SODIUM SULFITE (UNII: VTK01UQK3G)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-000-00	1 in 1 CARTON	12/01/1990
1		57 g in 1 TUBE; 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	12/01/1990

Labeler - J. Strickland & Co. (007023112)

Registrant - J. Strickland & Co. (007023112)

Establishment
Name	Address	ID/FEI	Business Operations
J. Strickland & Co.		007023112	manufacture(12022-000) , pack(12022-000) , label(12022-000)