Active Ingredients
APIS MELLIFERA VENOM、MENTHA PIPERITA LEAF、 TOCOPHEROL
South Moon Psoriasis
FDA Label NDC 84744-061
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Ouhoe Biotechnology Co., Ltd. for the product South Moon Psoriasis (NDC 84744-061). 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 active ingredients, purpose, use, warnings, otc - keep out of reach of children, stop use, do not use, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Relieve scaly erythema and itching of psoriasis; inhibit the growth ofpsoriasis, tinea pedisfungus; moisturize the skin and promote skin healing
Use
Take an appropriate amount of this product and apply it evenly to the affected area and massage to promote absorption.
Warnings
Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.
Otc - Keep Out Of Reach Of Children
Please keep out of reach of children. Do not swallow.
Stop Use
Discontinue use if signs of irritation or rash occur.
Do Not Use
Discontinue use if signs of irritation or rash occur.
Storage And Handling
Store in a cool and dry place.
Inactive Ingredient
GLYCERIN、ALLANTOIN
Package Label.Principal Display Panel
Label (So B06 0038 01)
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