Otc - Active Ingredient
Active ingredient: atractylodis rhizoma
Stomint
FDA Label NDC 42469-2001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Evercarepharm Co., Ltd for the product Stomint (NDC 42469-2001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredient: hovenia dulcis thunberg, crataegi fructus, puerariae radix, glycyrrhizae resina, agastachis herba, scutellariae radix, cinnamon bark
Otc - Purpose
For the treatment of reflux esophagitis, chronic gastritis, acute gastritis, abdominal distension, indigestion, hangovers
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Take 3 times a day after meals with warm water
Warnings
Keep in a dry, cool placekeep away from direct sunlight
Dosage & Administration
Do not take if you are pregnant
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