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

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Golden Medicated

Kutol Products Company, Inc.

Golden Medicated




FULL PRESCRIBING INFORMATION

Active ingredient

Chloroxylenol 0.3% w/w.......Antibacterial Handwashing

Water, Tall Oil Acid, Potassium Hydroxide, Sodium Lauryl Sulfate, Coconut Acid, Cocamide DIPA, Phenoxyethanol, Tetrasodium EDTA, Sodium Sulfate, Sodium Laureth Sulfate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Iodopropynyl Butylcarbamate, Fragrance, Red 33, Yellow 5.

Purpose

Handwash to help decrease bacteria on the skin.

For external use only.

Do not use in the eyes. In case of contact, immediately flush with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

  • Apply a small amount, covering hands with product for 30 seconds. Add water, lather and rinse.
  • Children under 6 years of age should be supervised when using this product.

Uses

Handwash to help decrease bacteria on the skin.

Do not use in the eyes. In case of contact, immediately flush with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

Golden Medicated  50865-060-09.jpg

Golden Medicated  50865-060-27.jpg

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

Golden Medicated

Medicated Lotion Soap SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50865-060
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chloroxylenol Chloroxylenol 0.3 g

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM HYDROXIDE
coconut acid
SODIUM LAURYL SULFATE
PHENOXYETHANOL
SODIUM LAURETH SULFATE
IODOPROPYNYL BUTYLCARBAMATE
SODIUM SULFATE
D&C RED NO. 33
FD&C YELLOW NO. 5
EDETATE SODIUM
TALL OIL ACID
Aloe Vera Leaf
.ALPHA.-TOCOPHEROL ACETATE
COCO DIISOPROPANOLAMIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50865-060-09 3785 in 1 BOTTLE, PLASTIC
2 NDC:50865-060-27 1000 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2014-03-11


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