KENDALL SOOTHING- zinc oxide ointment

Kendall Soothing by

Drug Labeling and Warnings

Kendall Soothing by is a Otc medication manufactured, distributed, or labeled by Covidien Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Zinc oxide 10%

PURPOSE

Purpose

Skin protectant

INDICATIONS & USAGE

Use

temporarily protects chapped or cracked skin.

WARNINGS

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.

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

Directions

• apply as needed
  

SPL UNCLASSIFIED SECTION

Other Information

• protect from freezing
• avoid excessive heat
  

INACTIVE INGREDIENT

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

Questions or comments?  1-800-962-9888

PRINCIPAL DISPLAY PANEL

Image of Kendall Soothing Ointment 2 Fl oz Label

INGREDIENTS AND APPEARANCE

KENDALL SOOTHING 
zinc oxide ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 28851-695
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc - UNII:J41CSQ7QDS)	Zinc Oxide	10 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BERGAMOT OIL (UNII: 39W1PKE3JI)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ACETATE ION (UNII: 569DQM74SC)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
JOJOBA OIL (UNII: 724GKU717M)
POLYSORBATE 60 (UNII: CAL22UVI4M)
1-DECENE (UNII: 7O4U4C718P)
XANTHAN GUM (UNII: TTV12P4NEE)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 28851-695-01	59 mL in 1 TUBE
2	NDC: 28851-695-02	118 mL in 1 TUBE
3	NDC: 28851-695-03	4 mL in 1 POUCH

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)