Label: KENDALL MOISTURIZING- dimethicone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 28851-694-01, 28851-694-02, 28851-694-03 - Packager: Covidien Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated April 27, 2011
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
When using this product
- do not get into eyes
- deep or puncture wounds
- animal bites
- serious burns
- condition worsens
- symptoms last more than seven days or clear up and occur again within a few days
- do not get into eyes
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
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INACTIVE INGREDIENT
Inactive ingredients
Water, simmondsia chinensis (jojoba) seed oil, zea mays (corn) starch, cetearyl alcohol, glyceryl stearate, cirtus aurantium bergamia (bergamot) fruit oil, citrus medica vulgaris peel oil, sodium stearoyl lactylate, retinyl palmitate, tocopheryl acetate, isopropyl palmitate, propylene glycol, triethanolamine, sodium PCA, carbopol, butyrospermum parkii (shea butter), decylene glycol, phenoxyethanol, methylparaben, butylparaben, propylparaben, isobutylparaben, ethylparaben
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KENDALL MOISTURIZING
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:28851-694 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O) Dimethicone 1.5 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) JOJOBA OIL (UNII: 724GKU717M) STARCH, CORN (UNII: O8232NY3SJ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) PHENOXYETHANOL (UNII: HIE492ZZ3T) BERGAMOT OIL (UNII: 39W1PKE3JI) TROLAMINE (UNII: 9O3K93S3TK) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CARBOMER 1342 (UNII: 809Y72KV36) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) 1-DECENE (UNII: 7O4U4C718P) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLPARABEN (UNII: 3QPI1U3FV8) PROPYLPARABEN (UNII: Z8IX2SC1OH) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) ETHYLPARABEN (UNII: 14255EXE39) SHEA BUTTER (UNII: K49155WL9Y) ACETATE ION (UNII: 569DQM74SC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:28851-694-01 59 mL in 1 TUBE 2 NDC:28851-694-02 118 mL in 1 TUBE 3 NDC:28851-694-03 4 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 04/20/2011 Labeler - Covidien Inc. (805770828)
