61096-2007 : Sprayology Travelease Oral Liquid


NDC61096-2007
Labeler: Eight and Company L.L.C
Product Type: Human OTC Drug
Drug Name: Sprayology Travelease
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 61096-2007-1: 1 BOTTLE, SPRAY IN 1 CARTON (61096‑2007‑1) > 41 ML IN 1 BOTTLE, SPRAY

Active Ingredients:

  • Apis Mellifera
  • Activated Charcoal
  • Milk Thistle
  • Anamirta Cocculus Seed
  • Strychnos Ignatii Seed
  • Strychnos Nux-vomica Seed
  • Passiflora Incarnata Flowering Top
  • Tobacco Leaf

Dosage Strength:

  • 200 [hp_C]/41mL
  • 200 [hp_C]/41mL
  • 4 [hp_X]/41mL
  • 30 [hp_C]/41mL
  • 200 [hp_C]/41mL
  • 30 [hp_C]/41mL
  • 4 [hp_X]/41mL
  • 6 [hp_X]/41mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Allergens [CS]
  • Bee Venoms [CS]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Plant Proteins [CS]
  • Seed Storage Proteins [CS]
  • Standardized Insect Venom Allergenic Extract [EPC]

Related Products:

Based on records with the same trade name.
  • 61096-0007 Sprayology Travelease Oral Liquid by Eight and Company
  • 61096-1007 Sprayology Travelease Oral Liquid by Eight and Company

NDC QR Code

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NDC 61096-2007 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.