Ultra Glow Fade
Medically reviewed by Drugs.com. Last updated on Dec 24, 2020.
Dosage form: cream
Ingredients: HYDROQUINONE 2g in 102g, PADIMATE O 1.5g in 102g
Labeler: Keystone Laboratories
NDC Code: 58318-008
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
2% Hydroquinone ..... Skin Lightener
1.5% Padimate O.......Subscreen
Keep out of reach of children.
For external use only. Children under 12 years of age: Do not use unless directed by a doctor. Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor. Avoid contact with eyes, rinse with water to remove. Sun exposure should be limited by using a sunscreen agent, a sun blocking agent, or protective clothing to cover bleached skin during and after treatment is completed in order to prevent darkening from reoccurring. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adults: Apply a small amount in a thin layer on the affected area twice daily or as directed by a doctor. If no improvement is seen after 3 months of treatment, use of this product should be discontinued. Lightening effect of this product may not be noticeable on very dark skin.
Other Information: Protect the product in this container from excessive heat and direct sun. For expiration date, please see bottom of jar.
KEYSTONE LABORATORIES © 2013
1-800-772-8860 / Memphis, TN 38101-2026
MADE IN U.S.A.
water, stearyl stearate, propylene glycol, cetyl alcohol, isopropyl myristate, mineral oil, sodium metabisulfite, fragrance, steareth 20, methylparaben, butylhydoxytoluene, prophyl gallate, sodium sulfite, sodium sulfite, tetrasodium EDTA, propylparaben, citric acid, aloe barbadensis (Leaf Juice)
|ULTRA GLOW FADE
|Labeler - Keystone Laboratories (007017429)|