Kendall Soothing

Dosage form: ointment
Ingredients: Zinc Oxide 10mL in 100mL
Labeler: Covidien Inc.
NDC Code: 28851-695

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.

Kendall Soothing Ointment

Active Ingredient

Zinc oxide 10%

Purpose

Skin protectant

Use

temporarily protects chapped or cracked skin.

Warnings

For external use only.

When using this product 
  • do not get into eyes
Do not use on 
  • deep or puncture wounds
  • animal bites
  • serious burns
Stop use and ask a doctor if
  • condition worsens
  • symptoms last more than seven days or clear up and occur again within a few days.
Keep out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.



Directions

  • apply as needed

Other Information

  • protect from freezing
  • avoid excessive heat

Inactive ingredients

Water, Polysorbate 60, petrolatum, sorbitan stearate, cetyl alcohol, propylene glycol, dimethicone, simmondsia chinensis (jojoba) seed oil, decylene glycol, xanthan gum, cetyl hydroxyethylcellulose, citrus aurantium bergamia (bergamot) fruit oil, citrus medica vulgaris peel oil, retinyl palmitate, tocopheryl acetate, methylparaben, propylparaben, diazolidinyl urea

Questions or comments?  1-800-962-9888


Image of Kendall Soothing Ointment 2 Fl oz Label





KENDALL SOOTHING 
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:28851-695
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (Zinc) Zinc Oxide10 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water 
PETROLATUM 
SORBITAN MONOSTEARATE 
PROPYLENE GLYCOL  
BERGAMOT OIL  
VITAMIN A PALMITATE 
ACETATE ION 
METHYLPARABEN 
PROPYLPARABEN  
DIAZOLIDINYL UREA 
CETYL ALCOHOL 
DIMETHICONE 
JOJOBA OIL 
POLYSORBATE 60 
1-DECENE 
XANTHAN GUM 
CETYL HYDROXYETHYLCELLULOSE (350000 MW) 
Packaging
#Item CodePackage Description
1NDC:28851-695-0159 mL in 1 TUBE
2NDC:28851-695-02118 mL in 1 TUBE
3NDC:28851-695-034 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34704/22/2011
Labeler - Covidien Inc. (805770828)

Revised: 04/2011
 
Covidien Inc.

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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