GenRx Cala Zinc Skin Healing description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

GenRx Cala Zinc Skin Healing

PureTek Corporation


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Zinc Oxide 20.0%

(3.0% as Calamine)

Purpose

Skin Protectant

GenRx Cala Zinc Skin Healing Uses

■ for the treatment and/or prevention of diaper rash
■ temporarily protects and helps relieve minor skin irritation and itching due to rashes

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

■ cleanse skin with GenRx All Purpose Cleansing Lotion or Body Cleanser and apply paste to area as needed
■ for peri-G tubes, cleanse as above, apply thin layer and secure with drain sponge or product as directed

GenRx Cala Zinc Skin Healing Other information

■ protect from freezing    ■ avoid excessive heat

Inactive ingredients

Aleurites moluccana seed oil, Aloe barbadensis (Aloe vera) leaf juice, Carthamus tinctorius (safflower) seed oil, fragrance, 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], modified corn starch, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, petrolatum, phenoxyethanol, sodium hyaluronate.

Cala Zinc Skin Healing Paste with GenRx Complex (4 oz tube label)

GenRx Cala Zinc Skin Healing

GenRx Cala Zinc Skin Healing

Zinc Oxide PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59088-852
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 200 mg

Inactive Ingredients

Ingredient Name Strength
KUKUI NUT OIL
Aloe Vera Leaf
SAFFLOWER OIL
LEVOMENOL
CALCIUM PANTOTHENATE
Carthamus Tinctorius Seed Oleosomes
maltodextrin
NIACINAMIDE
PYRIDOXINE HYDROCHLORIDE
SILICON DIOXIDE
SODIUM ASCORBYL PHOSPHATE
.ALPHA.-TOCOPHEROL ACETATE, DL-
GINGER
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)
petrolatum
PHENOXYETHANOL
HYALURONATE SODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59088-852-01 4 in 1 POUCH
2 NDC:59088-852-08 118 in 1 TUBE

Marketing Information

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


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.