Quick answers
- What is Artemisia argyi leaf used for?
- The Drug Facts label of OUHOE Sun Milk (Shantou Ouhoe Technology Co., Ltd.) lists these uses: Spray and massage evenly onto the skin at least half an hour before sun exposure. For application on the face, first spray the product on your hands and then massage gently. Repeat the application frequently, especially after sweating, swimming or drying your skin with a towel..
- Do I need a prescription for Artemisia argyi leaf?
- 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 ingredient, 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 Artemisia argyi leaf 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.
OUHOE Sun Milk · Shantou Ouhoe Technology Co., Ltd.
Artemisia argyi leaf 0.01 mg/100 mg, spray (topical)
Active ingredient
ARTEMISIA ARGYI LEAF EXTRACT
Purpose
1. Effectively prevents UV damage to the skin. 2. Provides efficient sun protection to prevent sunburn. 3. Contains pomegranate extract to nourish the skin. 4. Lightweight formula, the skin is refreshed and non-sticky after use.
Uses
Spray and massage evenly onto the skin at least half an hour before sun exposure. For application on the face, first spray the product on your hands and then massage gently. Repeat the application frequently, especially after sweating, swimming or drying your skin with a towel.
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. Spray and massage evenly onto the skin at least half an hour before sun exposure. For application on the face, first spray the product on your hands and then massage gently. Repeat the application frequently, especially after sweating, swimming or drying your skin with a towel.
Directions
Spray and massage evenly onto the skin at least half an hour before sun exposure. For application on the face, first spray the product on your hands and then massage gently. Repeat the application frequently, especially after sweating, swimming or drying your skin with a towel.
Inactive ingredients
AQUA、GLYCERIN、MINERAL OIL、ACRYLATES COPOLYMER、PEG-100 STEARATE、TITANIUM DIOXIDE、MILK
— FDA label of OUHOE Sun Milk, Shantou Ouhoe Technology Co., Ltd., effective December 26, 2025. See the official label on DailyMed →
WOODSLEEP Sunscreen Balm · Shantou Woodsleep Biotechnology Co., Ltd.
Artemisia argyi leaf 0.012 mg/60 mg, cream (topical)
Active ingredient
ARTEMISIA ARGYI LEAF EXTRACT
Purpose
1. Helps prevent ultraviolet rays and prevent skin aging and sunburn due to sun exposure. 2. The texture is light and easy to apply evenly without leaving traces, allowing you to enjoy fresh and non-greasy skin. 3. The ingredients are mild, not irritating to the skin, and suitable for all types of skin.
Uses
1. Clean skin and keep it dry 2. Take an appropriate amount of this product and apply it evenly on the desired skin 3. Massage gently for complete 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. 1. Clean skin and keep it dry 2. Take an appropriate amount of this product and apply it evenly on the desired skin 3. Massage gently for complete absorption.
Directions
1. Clean skin and keep it dry 2. Take an appropriate amount of this product and apply it evenly on the desired skin 3. Massage gently for complete absorption.
Inactive ingredients
AQUA、ETHYLHEXYL METHOXYCINNAMATE、OCTOCRYLENE、ISONONYL ISONONANOATE、GLYCERYL STEARATE、TITANIUM DIOXIDE
— FDA label of WOODSLEEP Sunscreen Balm, Shantou Woodsleep Biotechnology Co., Ltd., effective December 13, 2025. 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 ingredient, 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.
Artemisia argyi leaf 0.01 mg/100 mg · spray (topical) · 2 products
Artemisia argyi leaf 0.012 mg/60 mg · cream (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| WOODSLEEP Sunscreen Balm | Shantou Woodsleep Biotechnology Co., Ltd. | DailyMed |
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 Ouhoe Technology Co., Ltd.2 products
- Shantou Woodsleep Biotechnology Co., Ltd.1 product
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.