58368-001 : Neorelief Topical Gel


NDC: 58368-001
Labeler: Biolyte Laboratories, LLC
Product Type: Human OTC Drug
Drug Name: Neorelief
Dosage Form: Topical Gel
Rev. Date: 


NDC Package Codes:

  • 58368-001-01: 56.7 G IN 1 TUBE (58368‑001‑01)

Active Ingredients:

  • Actaea Spicata Root
  • Althaea Officinalis Root
  • Arnica Montana
  • Atropa Belladonna Root
  • Bellis Perennis
  • Black Cohosh
  • Bryonia Alba Root
  • Calendula Officinalis Flowering Top
  • Caulophyllum Thalictroides Root
  • Causticum
  • Frangula Californica Bark
  • Guaiacum Officinale Resin
  • Horse Chestnut
  • Hypericum Perforatum
  • Ledum Palustre Twig
  • Lithium Carbonate
  • Potassium Carbonate
  • Rhododendron Aureum Leaf
  • Ruta Graveolens Flowering Top
  • Salicylic Acid
  • Stellaria Media
  • Toxicodendron Pubescens Leaf

Dosage Strength:

  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g
  • 4 [hp_X]/g

NDC QR Code

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NDC 58368-001 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.