Adrenalinum Pellet
Product Images NDC 0220-0078

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Adrenalinum (NDC 0220-0078). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

FDA Label Image

Label (Adrena200ck)

Label (Adrena200ck)
Adrenalinum 200 is a homeopathic medicine with an active ingredient that contains 0.443 mg of the component per pellet. The drug is made in France and is available only by prescription. It includes approximately 80 pellets and has a lot number and expiry date. The medicine is intended for adult and child use, and it is suggested to dissolve 5 pellets under the tongue 3 times a day or as directed by a physician until the symptoms are relieved. The drug also contains lactose and sucrose and should not be used if the pellet dispenser seal is broken. For more information about the drug and its usage, contact BoironUSA.com. If symptoms persist, it's recommended to ask a doctor.*
FDA Label Image

Adrenalinum 200ck Label

Adrenalinum 200ck Label
Adrenalinum 200 is a homoeopathic medicine made in France containing less than 10 mg of adrenaline per pellet. It comes in a container with around 80 pellets. The drug fact mentions it can be consumed as directed by a doctor or in case of symptoms, dissolve five pellets under the tongue three times a day until the symptoms resolve. It also advises not to use if the pellet dispenser seal is broken with lactose and sucrose as inactive ingredients. However, the text hints on how to disperse pellets.*

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