KERA HC Hydrocortisone description, usages, side effects, indications, overdosage, supplying and lots more!

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KERA HC Hydrocortisone

Clinical Therapeutic Solutions

KERA HC Cream Hydrocortisone 1%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KERA HC Cream Hydrocortisone 1%


Active Ingredient

Hydrocortisone-USP 1.00%

Purpose

Anti-Itch

Uses:


  • Excessively Dry Skin, Eczema, Insect Bites, Poison Ivy, Oak or Sumac, Soaps, Detergents, Cosmetics, Jewelery, Seborrheic Dermatitis, Psoriasis
  • Other uses of this product should only be under the advice and supervisor of a doctor

Warnings

  • For external use only

When using this product:

  • Avoid contact with eyes
  • Do not use more than directed unless told to do so by a doctor

Stop use and ask a doctor if:

  • Condition worsens or symptoms persist for more than 7 days, or if symptoms clear up, and then return

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately.


Store at room temperature (20-25 degrees C) (68-77 degrees F)


Directions:

For itching of skin irritation, inflammation and rashes:
  • Apply to affected area not more than 3 to  4 times daily.
  • Not for use by children under 2 years of age

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), C12-15 Alkyl Benzoate, c13-14 Isoparaffin, Ethylhexylglycerin, Glycerin, Heilianthus Annuus (Sunflower) Seed Oil, Laureth-7, Phenoxyethanol, Polacrylamide, Polysorbate-20, Tocopheryl Acetate (Vitamin E), Urea-USP.

Distributed By:

Clinical Therapeutic Solutions, PO Box 1257, Wall, NJ 07719  www.CTSRX.com

KERA HC Cream Hydrocortisone 1% 2oz/56g (44577-623-02)

KERA HC Hydrocortisone

KERA HC Hydrocortisone

HYDROCORTISONE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44577-623
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Hydrocortisone HYDROCORTISONE 1 g

Inactive Ingredients

Ingredient Name Strength
Aloe Vera Leaf
water
ALKYL (C12-15) BENZOATE
C13-14 ISOPARAFFIN
ETHYLHEXYLGLYCERIN
GLYCERIN
SUNFLOWER OIL
LAURETH-7
PHENOXYETHANOL
POLYSORBATE 20
.ALPHA.-TOCOPHEROL
UREA

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44577-623-02 56 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-10-17


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Be sure to consult your doctor before taking any medication!
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