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GenRx Cala Zinc Skin Healing

Dosage form: paste
Ingredients: ZINC OXIDE 200mg in 1mL
Labeler: PureTek Corporation
NDC Code: 59088-852

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient

Zinc Oxide 20.0%

(3.0% as Calamine)

Purpose

Skin Protectant

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

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​TM (4 oz tube label)

GENRX CALA ZINC SKIN HEALING 
zinc oxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-852
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:59088-852-69144 POUCH in 1 CARTON
1NDC:59088-852-014 mL in 1 POUCH
2NDC:59088-852-08118 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/08/2013
Labeler - PureTek Corporation (785961046)
Establishment
NameAddressID/FEIOperations
PureTek Corporation785961046manufacture(59088-852), pack(59088-852), label(59088-852)

Revised: 01/2013
 
PureTek Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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