Quick answers
- What is Shea butter used for?
- The Drug Facts label of FEELSHION Lavender Magnesium (Beijing JUNGE Technology Co., Ltd.) lists these uses: Skin.
- Do I need a prescription for Shea butter?
- 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 Shea butter 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.
FEELSHION Lavender Magnesium · Beijing JUNGE Technology Co., Ltd.
Shea butter 3%, cream (cutaneous)
Active ingredient
MAGNESIUM CHLORIDE,SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL,HYALURONIC ACID,VITIS VINIFERA (GRAPE) SEED OIL,TOCOPHEROL,LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL
Purpose
*Helps solve sleep problems *Promote deep relaxation *Relieve muscle tension*lmprove sleep quality
Uses
Skin
Warnings
For external use only. on damaged or broken skin. keep out of eyes. Rinse with water to remove. Please use this product before going to bed, apply thisproduct to the neck, shoulders, legs, etc, Gentlymassage for 5-10 seconds until completely absorbed. rash occurs. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply an appropriate amount of magnesium cream to the desired location.
Inactive ingredients
AQUA BUTYROSPERMUM PARKII (SHEA BUTTER) ALOE BARBADENSIS FLOWER EXTRACT SQUALANE COCOS NUCIFERA (COCONUT) OIL TREMELLA FUCIFORMIS POLYSACCHARIDE GLYCERIN ROSA MULTIFLORA FRUIT EXTRACT PANTHENOL SODIUM LACTATE BIOSACCHARIDE GUM-1 CHRYSANTHELLUM INDICUM EXTRACT PORTULACA OLERACEA EXTRACT HOUTTUYNIA CORDATA EXTRACT OPUNTIA TUNA FRUIT EXTRACT 1,2-HEXANEDIOL
— FDA label of FEELSHION Lavender Magnesium, Beijing JUNGE Technology Co., Ltd., effective May 14, 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.
Shea butter 3% · cream (cutaneous) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| FEELSHION Lavender Magnesium | Beijing JUNGE Technology 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.
- Beijing JUNGE Technology 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.