DIABETIC FOOT DEFENSE description, usages, side effects, indications, overdosage, supplying and lots more!

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DIABETIC FOOT DEFENSE

Genuine Virgin Aloe Corporation
Genuine Virgin Aloe Corporation




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENT

ALLANTOIN 1.5%

DIMETHICONE 1.5%

Purpose

PURPOSE:

SKIN PROTECTANT

Uses

Uses

  • temporarily protects minor
  • cuts
  • scrapes
  • burns
  • helps prevent and temporarily protect chafed, chapped or cracked skin

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

  • ON DEEP PUNCTURE WOUNDS
  • ON INFECTIONS
  • ON LACERATIONS

WHEN USING THIS PRODUCT

  • avoid contact with eyes

STOP USE AND ASK A DOCTOR IF

  • condition worsens or does not improve within 7 days

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

DIRECTIONS:

  • APPLY GENEROUSLY 1 TO 3 TIMES DAILY, OR AS DIRECTED BY A DOCTOR

Inactive ingredients aloe barbadensis (aloe vera) leaf extract, AP4® genuine virgin aloe complex, avena sativa (oat) kernel extract, beeswax,
butyrospermum parkii (shea butter), cetearyl alcohol (plant derived), cetyl alcohol (plant derived), ethylhexylglycerin (plant derived), gluconolactone (corn derived), lactic acid, panthenol (pro-vitamin B5), phenoxyethanol, polysorbate-60 (plant derived), sodium benzoate (plant derived), sodium hyaluronate, sodium lactate, urea, squalane, tetrasodium EDTA, tocopheryl acetate (vitamin E), zinc PCA

QUESTIONS?

CALL 800-279-7282

OR VISIT WWW.TRIDERMA.COM

DIABETIC FOOT DEFENSE

DIABETIC FOOT DEFENSE

DIABETIC FOOT DEFENSE

ALLANTOIN AND DIMETHICONE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10738-303
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALLANTOIN 0.5 g
DIMETHICONE 2 g

Inactive Ingredients

Ingredient Name Strength
Aloe Vera Leaf
Oatmeal
YELLOW WAX
SHEA BUTTER
CETOSTEARYL ALCOHOL
CETYL ALCOHOL
ETHYLHEXYLGLYCERIN
GLUCONOLACTONE
LACTIC ACID
PANTHENOL
PHENOXYETHANOL
POLYSORBATE 60
SODIUM BENZOATE
HYALURONATE SODIUM
sodium lactate
UREA
SQUALANE
EDETATE SODIUM TETRAHYDRATE
.ALPHA.-TOCOPHEROL ACETATE
Zinc Pidolate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10738-303-14 119 in 1 TUBE
2 NDC:10738-303-54 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2014-01-02


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Be sure to consult your doctor before taking any medication!
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