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Adenosine

The structure of adenosine was first described in 1931,[A229823] though the vasodilating effects were not described in literature until the 1940s. … [A229833,A229838] Adenosine is also indicated in the treatment of supraventricular tachycardia.[L31998] Adenosine was granted FDA approval on 30 October 1989.[L31978]

Ceftazidime

[L32935] Ceftazidime was approved by the FDA on July 19, 1985, and is currently available either alone or in combination with the non-β-lactam β-lactamase inhibitor [avibactam] to treat a variety of … Bacteria possess a cell wall comprising a glycopeptide polymer commonly known as peptidoglycan, which is synthesized and remodelled through the action of a family of enzymes known as "penicillin-binding

Dorzolamide

[L11377] It works by blocking an enzyme in the ciliary process that regulates ion balance and fluid pressure in the eyes. … Dorzolamide is a non-bacteriostatic sulfonamide derivative [A1304] and topical carbonic anhydrase (CA) inhibitor that treats elevated intraocular pressure (IOP) associated with open-angle glaucoma and

Kaolin

Until the early 1990s it was the active substance of anti-diarrhoea medicine Kaopectate.

Witch hazel

Betula pendula tar oil

The origin plant, also known as the European white or silver birch, grows mainly in the northern hemisphere. … [L1113] By the FDA, it is considered under the substances approved to be added to the food.

Glycerin

A trihydroxy sugar alcohol that is an intermediate in carbohydrate and lipid metabolism.

Cefixime

[L49293] The beta-lactam ring of cefixime inhibits bacterial cell wall synthesis by binding to the penicillin-binding proteins which will then result in lysis. … [T894, T322] Additionally, third-generation cephalosporins have been shown to have more stability in the presence of beta-lactamases compared to first- and second-generation cephalosporins.

Mineral oil

(PAC) can lead to skin cancer. … Unrefined or mildly treated mineral oils are classified as Group 3 carcinogens by the World Health Organizations, as chronic exposure to these aromatics including alkylated polycyclic aromatic compounds

Esomeprazole

As the binding of esomeprazole to the (H+, K+)-ATPase enzyme is irreversible and new enzyme needs to be expressed in order to resume acid secretion, esomeprazole's duration of antisecretory effect persists … Esomeprazole is the s-isomer of [DB00338], which is a racemate of the S- and R-enantiomer.