ARTRA SKIN TONE FOR OILY SKIN- hydroquinone, homosalate, oxybenzone cream 
J. Strickland & Co.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Artra Skin Tone Cream for Oily Skin

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

12022-000-00

ARTRA SKIN TONE FOR OILY SKIN 
hydroquinone, homosalate, oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE75 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE20 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12022-000-001 in 1 CARTON12/01/199009/29/2020
157 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A12/01/199009/29/2020
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIBusiness Operations
J. Strickland & Co.007023112manufacture(12022-000) , pack(12022-000) , label(12022-000)

Revised: 11/2020
 
J. Strickland & Co.