Label: NO DENTAL CARE (IMPROVES GUM DISEASE, GUM HEALTH, BREATH)- nitric oxide, tri-calcium phosphate, dental type silica, tocopheryl acetate liquid
- NDC Code(s): 83202-9575-5
- Packager: HumanEnos LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 12, 2024
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- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- PURPOSE
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO DENTAL CARE (IMPROVES GUM DISEASE, GUM HEALTH, BREATH)
nitric oxide, tri-calcium phosphate, dental type silica, tocopheryl acetate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83202-9575 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE 100 mg in 150 mg Inactive Ingredients Ingredient Name Strength PROPOLIS WAX (UNII: 6Y8XYV2NOF) 1 mg in 150 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83202-9575-5 150 mg in 1 PACKAGE; Type 0: Not a Combination Product 02/13/2024 02/12/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/13/2024 02/12/2025 Labeler - HumanEnos LLC (695801540) Establishment Name Address ID/FEI Business Operations HumanEnos LLC 695801540 manufacture(83202-9575)