GenRx Ultra Therapeutic Skin Repairing description, usages, side effects, indications, overdosage, supplying and lots more!

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GenRx Ultra Therapeutic Skin Repairing

PureTek Corporation


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Dimethicone 5.0%

Purpose

Skin Protectant

GenRx Ultra Therapeutic Skin Repairing Uses

■ for the treatment and/or prevention of diaper rash
■ temporarily protects and helps relieve chapped or cracked skin

Warnings

For external use only

Do not use on

■ deep or puncture wounds    ■ animal bites    ■ serious burns

When using this product

■ do not get into eyes

Stop use and ask a doctor if

■ condition worsens
■ symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ apply cream liberally as needed

GenRx Ultra Therapeutic Skin Repairing Other information

■ protect from freezing    ■ avoid excessive heat

Inactive ingredients

Aleurites moluccana seed oil, Aloe barbadensis (Aloe vera) leaf juice, butylene glycol, caprylyl glycol, Carthamus tinctorius (safflower) seed oil, cetyl alcohol, chlorphenesin, dimethicone crosspolymer, disodium EDTA, fragrance, glycerin, glyceryl stearate, GenRx Complex™ [consisting of: bisabolol, calcium pantothenate (vitamin B5), Carthamus tinctorius (safflower) oleosomes, maltodextrin, niacinamide (vitamin B3), pyridoxine HCl (vitamin B6), silica, sodium ascorbyl phosphate (vitamin C), sodium starch octenylsuccinate, tocopheryl acetate (vitamin E), Zingiber officinale (ginger) root extract], PEG-100 stearate, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, purified water, sodium hyaluronate, stearic acid, triethanolamine.

Ultra Therapeutic Skin Repairing Cream with GenRx Complex (4 oz tube label)

GenRx Ultra Therapeutic Skin Repairing

GenRx Ultra Therapeutic Skin Repairing

Dimethicone CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59088-663
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIMETHICONE 50 mg

Inactive Ingredients

Ingredient Name Strength
KUKUI NUT OIL
Aloe Vera Leaf
BUTYLENE GLYCOL
CAPRYLYL GLYCOL
SAFFLOWER OIL
CETYL ALCOHOL
CHLORPHENESIN
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER
EDETATE DISODIUM
GLYCERIN
GLYCERYL MONOSTEARATE
LEVOMENOL
CALCIUM PANTOTHENATE
Carthamus Tinctorius Seed Oleosomes
maltodextrin
NIACINAMIDE
PYRIDOXINE HYDROCHLORIDE
SILICON DIOXIDE
SODIUM ASCORBYL PHOSPHATE
.ALPHA.-TOCOPHEROL ACETATE, DL-
GINGER
PEG-100 STEARATE
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)
PHENOXYETHANOL
water
HYALURONATE SODIUM
STEARIC ACID
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59088-663-08 118 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2013-01-08


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