Canker Complete description, usages, side effects, indications, overdosage, supplying and lots more!

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Canker Complete

Wasatch Product Development

Canker Complete




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                              Purpose 

Menthol 0.5%                                  Oral Pain Reliever               

Purpose

Uses        For the temporary relief of pain associated with canker and mouth sores

Keep this and all drugs out of reach of children

Uses

Stop use and ask a dentist or physician if

- Sore mouth symptoms do not improve in 7 days

- Irritation, pain or redness worsens

- Swelling, rash or fever develops

Do not use this product for more than 7 days unless directed by a health professional

Directions

Adults and children 2 years and older              Gently dab medication on the site of irritation with a cotton swab or fingertip

                                                                   Apply to the affected area up to 4 times a day, or as directed by a dentist or physician


Children under 12 years                               Adult supervision should be given in the use of this product

Children under 2 years                                 Consult dentist or physician

Inactive ingredients:

Calcium/Sodium PVM/MA Copolymer, TX-Factor 5 tm (propietary polypeptide lipid blend), Cellulose Gum, Mineral Oil,  Petrolatum, Lecithin, Chlorella Vulgaris  Extract, Hydrolyzed Lupine Protein, Silica, C12-15 Alkyl  Benzoate, Tribehenin, Ceramide 2, PEG-10 Rapeseed Sterol, Tetrasodium EDTA, Flavor, Melaleuca Alternafolia (Tea Tree) Leaf Oil, Caprylyl Glycol, Stearyl Glycyrrhetinate, Sucralose, DC Red Lake 27

Canker Complete

Canker Complete   Net wt. .21oz (6g)

Canker Complete

Canker Complete

Menthol CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44717-890
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 0.5 g

Inactive Ingredients

Ingredient Name Strength
CARBOXYMETHYLCELLULOSE SODIUM
Mineral Oil
petrolatum
EDETATE SODIUM
CAPRYLYL GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44717-890-01 6 in 1 TUBE
2 NDC:44717-890-02 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2010-10-11


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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