0067-6296 : Lamisil .84 g/125ml Topical Aerosol, Spray


NDC: 0067-6296
Labeler: Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
Product Type: Human OTC Drug
Drug Name:  Lamisil At
Dosage Form: Topical Aerosol, Spray
Application #: NDA021124
Rev. Date: 


NDC Package Codes:

  • 0067-6296-01: 125 ML IN 1 CAN (0067‑6296‑01)

Active Ingredients:

  • Terbinafine Hydrochloride

Dosage Strength:

  • .84 g/125mL

Pharmaceutical Classes:

  • Allylamine Antifungal [EPC]
  • Allylamine [CS]

Related Products:

Based on records with the same trade name.
  • 0067-6297 Lamisil .84 g/125ml Topical Aerosol, Spray by Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
  • 0067-3998 Lamisil 10 mg/g Topical Cream by Novartis Consumer Health, Inc.
  • 0067-4000 Lamisil At 1 ml/100ml Topical Spray by Novartis Consumer Health, Inc.
  • 0067-6171 Lamisil 10 mg/g Topical Cream by Novartis Consumer Health, Inc.
  • 0067-8100 Lamisil At 1 g/100g Topical Cream by Novartis Consumer Health, Inc.
  • 70518-1736 Lamisil At 1 g/100g Topical Cream by Remedyrepack Inc.

NDC QR Code

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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.