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Dermamine

Natureplex LLC

Dermamine Extra Strength Itch Stopping Cream


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purposes
Diphenhydramine Hydrochloride 2% Topical Analgesic
Zinc Acetate 0.1% Skin Protectant

Dermamine Uses

  • Temporarily relieves pain and itching associated with:
    • insect bites
    • minor burns
    • sunburn
    • scrapes
    • minor skin irritations
    • minor cuts
    • rashes due to poison ivy, poison oak and poison sumac
  • dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings

For external use only

Do not use

  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

When using this product avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens or does not improve within 7 days
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of the reach of children. In case of accidental ingestion, seek medical attention right away or contact a Poison Control Center immediately.

Directions

  • do not use more than directed
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

Dermamine Other information

  • store between 15° and 30° C (59° and 86° F)
  • close cap tightly after use
  • do not use if seal on tube is punctured or missing

Inactive ingredients

DMDM Hydantoin, GMS, isopropyl myristate, light mineral oil, methylparaben, propylparaben, ritacol, purified water

Questions or comments?

1-866-323-0107

PRINCIPAL DISPLAY PANEL - 35 g Tube Box

EXTRA STRENGTH

BLOCKS
THE ITCH-CAUSING
HISTAMINES

Natureplex

Dermamine
Itch Stopping
Cream
Topical Analgesic Skin Protectant

NDC 67234-023-01

NET WT. 1.25 Oz.(35g)

Dermamine

Dermamine

DIPHENHYDRAMINE and ZINC ACETATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67234-023
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE DIPHENHYDRAMINE 0.02 mg
ZINC ACETATE zinc 0.001 U

Inactive Ingredients

Ingredient Name Strength
DMDM HYDANTOIN
GLYCERYL 1-STEARATE
ISOPROPYL MYRISTATE
LIGHT MINERAL OIL
METHYLPARABEN
PROPYLPARABEN
CETOSTEARYL ALCOHOL
POLYSORBATE 60
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 35 in 1 TUBE
2 NDC:67234-023-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-03-01


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