49410-200 : Teeth Desensitizing and Remineralizing Gel Dental Paste


NDC49410-200
Labeler: Fuzhou Difeng Bio-tech Co., Ltd.
Product Type: Human OTC Drug
Drug Name: Teeth Desensitizing and Remineralizing Gel
Dosage Form: Dental Paste
Application #: part356
Rev. Date: 


NDC Package Codes:

  • 49410-200-01: 5 CONTAINER IN 1 CARTON (49410‑200‑01) > 200 VIAL, SINGLE‑USE IN 1 CONTAINER > 1.5 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-02: 5 CONTAINER IN 1 CARTON (49410‑200‑02) > 100 VIAL, SINGLE‑USE IN 1 CONTAINER > 2 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-03: 5 CONTAINER IN 1 CARTON (49410‑200‑03) > 100 VIAL, SINGLE‑USE IN 1 CONTAINER > 4 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-04: 5 CONTAINER IN 1 CARTON (49410‑200‑04) > 80 VIAL, SINGLE‑USE IN 1 CONTAINER > 6 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-05: 6 CONTAINER IN 1 CARTON (49410‑200‑05) > 300 VIAL, SINGLE‑USE IN 1 CONTAINER > 4.5 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-06: 6 CONTAINER IN 1 CARTON (49410‑200‑06) > 200 VIAL, SINGLE‑USE IN 1 CONTAINER > 10 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-07: 6 CONTAINER IN 1 CARTON (49410‑200‑07) > 333 VIAL, SINGLE‑USE IN 1 CONTAINER > 3 G IN 1 VIAL, SINGLE‑USE
  • 49410-200-08: 300 VIAL, SINGLE‑USE IN 1 CARTON (49410‑200‑08) > 3.5 G IN 1 VIAL, SINGLE‑USE

Active Ingredients:

  • Potassium Nitrate
  • Sodium Fluoride

Dosage Strength:

  • 50 mg/g
  • 1.5 mg/g

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.