Vax Sode Spray
Product Images NDC 83027-0071

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Vax Sode (NDC 83027-0071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nutritional Specialties, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Vax-sode (Nspc0080 Vax Sode)

Vax-sode (Nspc0080 Vax Sode)
This product is for professional use only. It contains homeopathic ingredients and is not evaluated by the FDA. The active ingredients include Thuja Occidentalis, Calcarea Carbonica, Silicea, Salmonella Typhi Nosode, Serum Anguillag, Bacillus Tetani, Malandrinum, Morbillinum, Parotidinum, Rubella Nosode, Yersinia Enterocolitica, and Salmonella Enteriditis. It is indicated for temporary relief of symptoms such as sweats, chills, muscle and joint aches, fatigue, and headache. The recommended dosage is 2 to 3 sprays orally, three times daily for adults, and half of the adult dosage for children under twelve. It can also be rubbed on the skin at pulse points or abdomen. It should not be taken within 15 minutes of consuming food, beverage, or brushing teeth. The product should be stored in a cool place after opening and kept out of reach of children. If pregnant or breastfeeding, it is important to consult a health professional before use. If there is an overdose, medical help or contact with a Poison Control Center should be sought. In case of worsening condition, medical attention should be sought. It should not be used if the tamper evident seal is broken or missing. The product is manufactured exclusively for Nutritional Specialties, Inc.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.