KENDALL SOOTHING  - zinc oxide ointment 
Covidien Inc.

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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 Type HUMAN OTC DRUG NDC Product Code (Source) 28851-695 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (Zinc) Zinc Oxide 10 mL  in 100 mL

Inactive Ingredients Ingredient Name Strength 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)

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 28851-695-01 59 mL In 1 TUBE None 2 28851-695-02 118 mL In 1 TUBE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	04/22/2011

Labeler - Covidien Inc. (805770828)

Revised: 04/2011Covidien Inc.