Label: SOUTH MOON MAGNESIUM SOOTHING CREAM- glycerin cream
- NDC Code(s): 84983-018-01
- Packager: Shantou South Moon Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 27, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
PURPOSE
1. Deeply moisturize the skin, replenish the skin's moisture barrier and prevent moisture loss.
2. Enhance the skin's water-locking ability, repair and nourish the skin at night, so that the skin can be fully hydrated and moisturized during the rest period.
3. Enhance the hydration of the skin, keep the skin moist and plump for a long time, improve dryness and roughness, and make the skin look healthier and shiny.
- WHEN USING
- WARNINGS
- DO NOT USE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SOUTH MOON MAGNESIUM SOOTHING CREAM
glycerin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84983-018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LAVENDER OIL (UNII: ZBP1YXW0H8) (LAVENDER OIL - UNII:ZBP1YXW0H8) LAVENDER OIL 0.12 mg in 120 mg MENTHA SUAVEOLENS LEAF (UNII: 1341ZC68MK) (MENTHA SUAVEOLENS LEAF - UNII:1341ZC68MK) MENTHA SUAVEOLENS LEAF 0.12 mg in 120 mg ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X) ALOE VERA LEAF 0.12 mg in 120 mg Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) 3.6 mg in 120 mg GLYCERIN (UNII: PDC6A3C0OX) 9.6 mg in 120 mg MAGNESIUM CHLORIDE (UNII: 02F3473H9O) 0.12 mg in 120 mg GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) 2.4 mg in 120 mg TROLAMINE (UNII: 9O3K93S3TK) 0.24 mg in 120 mg CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC) 0.24 mg in 120 mg 1,2-HEXANEDIOL (UNII: TR046Y3K1G) 0.6 mg in 120 mg ALLANTOIN (UNII: 344S277G0Z) 0.12 mg in 120 mg WATER (UNII: 059QF0KO0R) 102.72 mg in 120 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84983-018-01 120 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/05/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M014 11/05/2025 Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192) Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192) Establishment Name Address ID/FEI Business Operations Shantou South Moon Biotechnology Co., Ltd. 457126192 manufacture(84983-018)

