Label: LIQUID liquid
- NDC Code(s): 84067-485-01
- Packager: Shantou Youjia E-Commerce Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated March 15, 2024
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INGREDIENTS AND APPEARANCE
LIQUID
liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84067-485 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 7.5 mg in 30 mg ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN) (ANGELICA SINENSIS WHOLE - UNII:697D19QDBN) ANGELICA SINENSIS WHOLE 9 mg in 30 mg PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) (PANAX GINSENG WHOLE - UNII:9L5JEP7MES) PANAX GINSENG WHOLE 4.5 mg in 30 mg REYNOUTRIA MULTIFLORA WHOLE (UNII: 85S46HFR8A) (REYNOUTRIA MULTIFLORA WHOLE - UNII:85S46HFR8A) REYNOUTRIA MULTIFLORA WHOLE 6 mg in 30 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 3 mL in 30 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84067-485-01 30 mg in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product 02/01/2024 12/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 02/01/2024 12/31/2024 Labeler - Shantou Youjia E-Commerce Co., Ltd. (711173127) Establishment Name Address ID/FEI Business Operations Shantou Youjia E-Commerce Co., Ltd. 711173127 label(84067-485)
