Label: CANKER CARE PLUS- menthol, unspecified form liquid
- NDC Code(s): 70084-500-01
- Packager: Quantum, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 February 6, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
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Warnings
Do not use this product for more than 7 days unless directed by a health professional. If sore mouth symptoms do not improve in 7 days; if irritation, pain or redness worsens; or if swelling, rash or fever develops; see your doctor or dentist. Do not exceed recommended dosage. Avoid contact with eyes.
- Directions
- Other Information
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Inactive Ingredients
Aloe Barbadensis Leaf Juice (Aloe Vera Gel), Calendula Officinalis Extract, Cellulose Gum, Commiphora Myrrha (Myrrh) Extract, Cyanocobalamin (Vitamin B12), Dipotassium Glyrrhizinate (DGL, Licorice), Echinacea Purpurea Extract, Eugenia Ceryophyllus (Clove Bud) Oil, Glycerine, Hydrastis Canadensis (Goldenseal) Leaf, Lysine, Melaleuca Alternifolia (Tea Tree) Oil, Melaleuca Leucadendron (Cajuputi) Oil, Mentha Piperita (Peppermint) Oil, Castor Oil, Polysorbate 20, Propolis Extract,Purified Water, Zinc
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 9.4 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
CANKER CARE PLUS
menthol, unspecified form liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70084-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A) Menthol, Unspecified Form 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength Echinacea Purpurea Whole (UNII: QI7G114Y98) TEA TREE OIL (UNII: VIF565UC2G) MELALEUCA CAJUPUTI LEAF OIL (UNII: 5O59RMR6DU) GOLDENSEAL (UNII: ZW3Z11D0JV) LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM) PROPOLIS WAX (UNII: 6Y8XYV2NOF) Water (UNII: 059QF0KO0R) Castor Oil (UNII: D5340Y2I9G) CYANOCOBALAMIN (UNII: P6YC3EG204) Zinc Gluconate (UNII: U6WSN5SQ1Z) Carboxymethylcellulose Sodium, Unspecified (UNII: K679OBS311) MYRRH (UNII: JC71GJ1F3L) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) CLOVE OIL (UNII: 578389D6D0) Glycerin (UNII: PDC6A3C0OX) Licorice (UNII: 61ZBX54883) Peppermint Oil (UNII: AV092KU4JH) Polysorbate 20 (UNII: 7T1F30V5YH) Calendula Officinalis Flower (UNII: P0M7O4Y7YD) Product Characteristics Color BROWN Score Shape Size Flavor MENTHOL Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70084-500-01 1 in 1 CARTON 04/01/2003 1 9.7 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part356 04/01/2003 Labeler - Quantum, Inc. (044806305)
