Artra Skin Tone Cream for Oily Skin

Manufacturer
J. Strickland & Co.
Effective date
2018-01-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:04:50

Label at a glance#

ProductArtra Skin Tone for Oily Skin
Active ingredientHYDROQUINONE, HOMOSALATE, OXYBENZONE
Label structure6 sections

Indications and uses

Gradually fades skin discolorations such as age spots freckles Liver spots dark areas that can occur while using oral contraceptives

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone, 7.5%

Homosalate, 2%

Oxybenzone, 2.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Skin Lightener

Sunscreen

Uses:

INDICATIONS & USAGE SECTION

Gradually fades skin discolorations such as

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

Warnings:

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • 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 

OTC - STOP USE SECTION

  • a gradual blue-black darking of the skin occurs
  • irritation becomes severe
  • no improvement is seen after 3 months

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

consult a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-000-0012022-000-00

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-00012022-000-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b34cb761-38bb-1232-e053-2a95a90a01dc6eef6b11-20c2-4665-a5dd-cce4e790102e2020-11-04WarningsExact identifier
spl set id: 6eef6b11-20c2-4665-a5dd-cce4e790102e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.