NDC 49589-199 Periactive

Sambucus Nigra Flower, Echinacea Purpurea, And Centella Asiatica

NDC Product Code 49589-199

NDC Code: 49589-199

Proprietary Name: Periactive Additional informationCallout TooltipWhat is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Sambucus Nigra Flower, Echinacea Purpurea, And Centella Asiatica Additional informationCallout TooltipWhat is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 49589 - Izun Pharmaceuticals Corp
    • 49589-199 - Periactive

NDC 49589-199-10

Package Description: 100 mL in 1 BOTTLE

NDC 49589-199-50

Package Description: 12 BOTTLE in 1 CARTON > 500 mL in 1 BOTTLE

NDC Product Information

Periactive with NDC 49589-199 is a a human over the counter drug product labeled by Izun Pharmaceuticals Corp. The generic name of Periactive is sambucus nigra flower, echinacea purpurea, and centella asiatica. The product's dosage form is mouthwash and is administered via topical form.

Labeler Name: Izun Pharmaceuticals Corp

Dosage Form: Mouthwash - An aqueous solution which is most often used for its deodorant, refreshing, or antiseptic effect.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Periactive Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SAMBUCUS NIGRA FLOWER 3 [hp_X]/mL
  • ECHINACEA PURPUREA 4 [hp_X]/mL
  • CENTELLA ASIATICA 4 [hp_X]/mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • SORBITOL (UNII: 506T60A25R)
  • SUCRALOSE (UNII: 96K6UQ3ZD4)
  • WATER (UNII: 059QF0KO0R)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)

Administration Route(s)

Additional informationCallout TooltipWhat are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Periactive Product Label Images

Periactive Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts:

Distributed By: straumannInstitut Straumann AG Peter Merian-Weg 12 | 4002 Basel | Switzerland

Otc - Purpose

  • Active Ingredients (in each 15ml)PurposesSambucus nigra 3xIrritation/gingivitis reducergum repair stimulator Echinacea purpurea 4xIrritation/gingivitis reducerHydrocotyle asiatica 4xIrritation/gingivitis reducer

Uses

  • Helps protect against gingivitisHelps reduce gum bleeding and sorenessHelps reduce plaque formationHelps reduce gum inflammationPromotes gingival healing

Allergy Alert

  • Do not use if allergic to any of the ingredients. Stop use and ask a dentist if:gingivitis, bleeding, or redness persists for more than 2 weeksyou have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be the signs of periodontitis, a serious form of gum disease.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children under 6 years of age.In case more than is used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 12 years and olderrinse for 60 seconds with 15ml (3 teaspoonful) twice a daychildren 6-12 yearsrinse for 60 seconds with 10ml (2 teaspoonful) twice a daychildren under 6 years of agedo not usedo not eat, drink or rinse your mouth for 30 minutes after usedo not swallowchildren 6 years to under 12 years of age: supervise use

Other Information

  • This rinse is not intended to replace brushing or flossingstore at room temperature 15-30°C (59-86°F)keep out of direct sunlight

Inactive Ingredients

Cetylpyridinium chloride, cool mint flavorcontains one or more of these ingredients, disodium EDTA, FD&C Blue No. 1 ,lactic acid, maltodextrin, menthol, nat. cinnamon flavor, PEG-40 hydrogenated castor oil, propylene glycol, sodium benzoate, sorbitol, sucralose, water, wintergreen flavor

Questions?

Call 1-800-956-2595

* Please review the disclaimer below.

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