Quick answers
- What is Aloe barbadensis leaf and sophora flavescens root used for?
- The Drug Facts label of SOHEJU Nail Repairs Patches (Shantou Ximonth Biotechnology Co., Ltd.) lists these uses: Wash and dry affected nails before going to bed. Open the package, take out the patch and tear off the back film. Place the patch on the nail and remove it after about 6-8 hours..
- Do I need a prescription for Aloe barbadensis leaf and sophora flavescens root?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Aloe barbadensis leaf and sophora flavescens root been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
SOHEJU Nail Repairs Patches · Shantou Ximonth Biotechnology Co., Ltd.
Aloe barbadensis leaf 0.006 mg/60 mg · Sophora flavescens root 0.006 mg/60 mg, patch (topical)
Active ingredient
SOPHORA ANGUSTIFOLIA ROOT EXTRACT, ALOE BARBADENSIS EXTRACT
Purpose
Nail Regeneration Reduces Discoloration Improves Cracked & Brittle Nails Removes & Prevents Nail Fungus Smooths And Hydrates Nail
Uses
Wash and dry affected nails before going to bed. Open the package, take out the patch and tear off the back film. Place the patch on the nail and remove it after about 6-8 hours.
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. Wash and dry affected nails before going to bed. Open the package, take out the patch and tear off the back film. Place the patch on the nail and remove it after about 6-8 hours.
Directions
Wash and dry affected nails before going to bed. Open the package, take out the patch and tear off the back film. Place the patch on the nail and remove it after about 6-8 hours.
Inactive ingredients
AQUA, GLYCERIN, ALLANTOIN
— FDA label of SOHEJU Nail Repairs Patches, Shantou Ximonth Biotechnology Co., Ltd., effective July 9, 2026. See the official label on DailyMed →
Nail Repairs Patches · Shantou Ximonth Biotechnology Co., Ltd.
Aloe barbadensis leaf 0.012 mg/60 mg · Sophora flavescens root 0.012 mg/60 mg, patch (topical)
Active ingredient
SOPHORA ANGUSTIFOLIA ROOT EXTRACT、ALOE BARBADENSIS EXTRACT
Purpose
1. A variety of moisturizing ingredients are absorbed into nails and skin through the patch, deeply nourishing, hydrating brittle nails, and reducing the appearance of thick and discolored nails. 2. Replenish nails with necessary moisture and nutrients, quickly reduce brittle manicure overnight, and restore manicure to show its natural, healthy appearance. 3. Hygienic material support, soft and strong, can provide gentle repair to nails. 4. The packaging is compact and easy to use. The patch design is suitable for carrying when going out and can be used anytime and anywhere.
Uses
1. Wash and dry affected nails before going to bed 2. Open the package, take out the patch and tear off the back film 3. Place the patch on the nail and remove it after about 6-8 hours
Warnings
Keep out of reach of children
Avoid contact with eyes.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place. 1. Wash and dry affected nails before going to bed 2. Open the package, take out the patch and tear off the back film 3. Place the patch on the nail and remove it after about 6-8 hours
Directions
1. Wash and dry affected nails before going to bed 2. Open the package, take out the patch and tear off the back film 3. Place the patch on the nail and remove it after about 6-8 hours
Inactive ingredients
AQUA、GLYCERIN、ALLANTOIN
— FDA label of Nail Repairs Patches, Shantou Ximonth Biotechnology Co., Ltd., effective January 16, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Aloe barbadensis leaf 0.006 mg/60 mg · Sophora flavescens root 0.006 mg/60 mg · patch (topical) · 2 products
Aloe barbadensis leaf 0.012 mg/60 mg · Sophora flavescens root 0.012 mg/60 mg · patch (topical) · 2 products
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Shantou Ximonth Biotechnology Co., Ltd.4 products
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.