70797-230 : Nuby Teething Gel 13 mg/g Topical Gel


NDC: 70797-230
Labeler: Talbot’s Pharmaceuticals Family Products, LLC.
Product Type: Human OTC Drug
Drug Name: Nuby Teething Gel
Dosage Form: Topical Gel
Application #: part356
Rev. Date: 


NDC Package Codes:

  • 70797-230-01: 24 CARTON IN 1 CARTON (70797‑230‑01) > 4 BLISTER PACK IN 1 CARTON > 1 TUBE IN 1 BLISTER PACK > 15 G IN 1 TUBE (70797‑230‑15)
  • 70797-230-24: 24 CARTON IN 1 CARTON (70797‑230‑24) > 4 BLISTER PACK IN 1 CARTON > 1 TUBE IN 1 BLISTER PACK > 15 G IN 1 TUBE (70797‑230‑15)
  • 70797-230-25: 24 CARTON IN 1 CARTON (70797‑230‑25) > 4 BLISTER PACK IN 1 CARTON > 1 TUBE IN 1 BLISTER PACK > 15 G IN 1 TUBE (70797‑230‑15)
  • 70797-230-26: 24 CARTON IN 1 CARTON (70797‑230‑26) > 6 BOX IN 1 CARTON > 1 TUBE IN 1 BOX > 15 G IN 1 TUBE (70797‑230‑15)

Active Ingredients:

  • Eugenol

Dosage Strength:

  • 13 mg/g

Related Products:

Based on records with the same trade name.
  • 70797-231 Nuby Teething Gel 8 mg/g Topical Gel by Talbot’s Pharmaceuticals Family Products, LLC.
  • 71240-231 Nuby Teething Gel 8 mg/g Topical Gel by Ningbo Longwell Baby Products Co Ltd
  • 71552-231 Nuby Teething Gel 8 mg/g Topical Gel by Europharma Concepts Limited

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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.