BRIGHTEN description, usages, side effects, indications, overdosage, supplying and lots more!

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BRIGHTEN

CEN BEAUTY LLC
CEN BEAUTY LLC




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENT

ZINC OXIDE 15%

OCTINOXATE 6%

Purpose

PURPOSE

SUNSCREEN

Uses

USES

  • Lightens discolored skin such as freckles, age and liver spots or pigment in the skin that may occur from pregnancy or from the use of oral contraceptives

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

  • IF YOU HAVE VERY SENSITIVE SKIN

WHEN USING THIS PRODUCT

  • Keep out of eyes. Rinse with water to remove.

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

ASK A DOCTOR BEFORE USE

  • On children under 12 years of age
  • If you are pregnant, breastfeeding or intend to become pregnant within 3 months of use.

DIRECTIONS

  • Apply a thin layer on affected area twice daily or as directed by a doctor.
  • If no improvement is seen after 3 months treatment, discontinue use.
  • Lightening effect may not be noticeable when used on very dark skin.
  • Limit sun exposure during and after use to prevent darkening from reoccurring.
  • Use a sun blocking agent or protective clothing. This product is not for use in the prevention of sunburn.
  • Consult your physician before use.

Other Information

  • STORE AT 15-30°C (59-86°F)
  • PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

INGREDIENTS

aqua (water), cyclopentasiloxane, PEG-10 dimethicone, dimethicone, butylene glycol, cyclohexasiloxane, glycerin, carollina officinalis extract, algae extract, avena sativa (oat) kernel extract, angelica sinensis extract, 10-hydroxydecanoic acid, sebacic acid, 1,10-decanediol acid, betaine, dimethicone/vinyl dimethicone crosspolymer, lauryl PEG-9 polydimethylsiloxyethyl dimethicone, lecithin, dimethicone/PEG-10/15 crosspolymer, triethoxycaprylylsilane, decamethylcyclopentasiloxane, trifluoromethyl C1-C4 alkyl dimethicone, quaternium-90, bentonite, butylene glycol, sodium chloride, sodium citrate, ethylhexylglycerin, propylene carbonate, propylene glycol, potassium sorbate, methylisothiazolinone, iodopropynyl butylcarbamate, phenoxyethanol

BRIGHTEN BRIGHTEN

BRIGHTEN

HYDROQUINONE GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54272-301
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Hydroquinone HYDROQUINONE 2 g

Inactive Ingredients

Ingredient Name Strength
water
ASCORBIC ACID
ALLANTOIN
Aminomethylpropanol
GLYCERIN
OAT
ANGELICA SINENSIS WHOLE
BUTYLENE GLYCOL
10-hydroxydecanoic acid
1,10-DECANEDIOL
LECITHIN, SOYBEAN
EDETATE DISODIUM
LACTIC ACID
GLYCERETH-7 TRIMETHYL ETHER
ETHYLHEXYLGLYCERIN
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)
HYALURONATE SODIUM
SODIUM METABISULFITE
POTASSIUM SORBATE
XANTHAN GUM
PHENOXYETHANOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54272-301-11 30 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part358A 2013-02-21


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