Label: MEDACTIVE PATIENT FRIENDLY- stannous fluoride kit
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Contains inactivated NDC Code(s)
NDC Code(s): 49741-1007-1, 49741-1007-2, 49741-1007-3 - Packager: Integrate Oral Care, LLC.
- Category: HUMAN OTC DRUG LABEL
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 December 30, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
Use immediately after preparing the rinse as follows:
Adults and children 6 years of age and older:
- Place both thumbs on Blue Chamber No. 1 and Press down firmly to squeeze fluoride into Chamber No. 2.
- Gently Shake.
- Snap Tab to Open by bending at line on the cap. Dispense half of mixture into the mouth and Rinse for 30 seconds. Spit.
- Gargle with remainder of mixture for 30 seconds. Spit.
- Avoid any food or drinks for at least 15 minutes after use.
Children under 6 years of age:
- Consult your medical doctor and/or dental professional
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDACTIVE PATIENT FRIENDLY
stannous fluoride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49741-1007 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49741-1007-2 10 in 1 BOX 07/31/2014 1 NDC:49741-1007-1 1 in 1 CARTON; Type 0: Not a Combination Product 2 NDC:49741-1007-3 30 in 1 BOX 07/31/2014 2 1 in 1 CARTON; Type 0: Not a Combination Product Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 KIT 3.7 mL Part 2 1 KIT 27 mL Part 1 of 2 CHAMBER NO. 1
stannous fluoride concentrateProduct Information Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 6.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) 1 mL in 1 mL GLYCERIN (UNII: PDC6A3C0OX) 1 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 3.7 mL in 1 KIT; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 07/31/2014 Part 2 of 2 CHAMBER NO. 2
stannous fluoride diluent emulsionProduct Information Route of Administration ORAL Inactive Ingredients Ingredient Name Strength SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) DIMETHICONE (UNII: 92RU3N3Y1O) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) POLOXAMER 407 (UNII: TUF2IVW3M2) SUCRALOSE (UNII: 96K6UQ3ZD4) WATER (UNII: 059QF0KO0R) EDETIC ACID (UNII: 9G34HU7RV0) Product Characteristics Color Score Shape Size Flavor RASPBERRY (Ruby Raspberry with ULTRAMULSION & Spilanthes Extract) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 27 mL in 1 KIT; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/31/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 07/31/2014 Labeler - Integrate Oral Care, LLC. (063540457) Registrant - Integrate Oral Care, LLC. (063540457)