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Ultra Glow Fade

Dosage form
CREAM
Labeler
Keystone Laboratories
Label updated
2018-01-10
Retrieved
2026-09-07
Active ingredients
HYDROQUINONE
View original label and images on DailyMed ↗
유효 성분

2% Hydroquinone ..... Skin Lightener

Label information

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

성분·작용

Skin lightener

효능·용도

Ultra Glow Fade Cream

2% Hydroquinone  ......  Skin Lightener

주의사항

Warnings:

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.

복용법·사용법

Directions:

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.

Label information

Other Information: Protect the product in this container from excessive heat and direct sun. For expiration date, please see bottom of jar.

Distributed by 

KEYSTONE LABORATORIES © 2013

www.keystone-labs.com

1-800-772-8860  / Memphis, TN 38101-2026

MADE IN U.S.A.

PM-LB 0011

첨가제

Inactive Ingredients:

Aqua/Water/Eau, Stearyl Stearate, Glycerol Stearate, Propylene Glycol Alcohol, Isopropyl Myristate, Sodium Metabisulfite, Fragrance, Sodium Sulfite, Steareth 20, Methyl Paraben, Buthydroxytoluene, Propyl Gallate, Tetrasodium EDTA, Propyl Paraben, Citric Acid

포장 표시

[Image in the official label — see DailyMed source]

DailyMed Set ID: 2557b4dc-2e85-4611-afed-c299f4ed3bbf · Version 5
NDC: 58318-003