Label: SLEEP GUMMIES chewable gel
- NDC Code(s): 83739-004-01
- Packager: XIAN CHIANG COMPANY LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 14, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When Using Section
- Stop Use Section
- Keep out of reach of childre
- Instructions
- Other information
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inactive ingredients
Egg Shell Collagen , Phytoceramides , Reishi Fruiting Body Extract ,Magnesium Bisglycinate , L-Theanine , Liposomal Apigenin ( from chamomile ) , GABA , Vitamin C , Liposomal Hyaluronic Acid , Valarian Root, Blue Passion Flower Extract , Lemon Balm Leaf Extract , Vitamin B6, Chelated Zinc Oxide , Copper , Melatonin.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SLEEP GUMMIES
sleep gummies chewable gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83739-004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BARLEY MALT (UNII: R3NBG8914U) (BARLEY MALT - UNII:R3NBG8914U) BARLEY MALT 1 g in 100 AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A) AMINO ACIDS 2 g in 100 Inactive Ingredients Ingredient Name Strength MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) VALERIAN (UNII: JWF5YAW3QW) CERAMIDE 2 (UNII: C04977SRJ5) REISHI (UNII: TKD8LH0X2Z) MAGNESIUM GLYCINATE (UNII: IFN18A4Y6B) ASCORBIC ACID (UNII: PQ6CK8PD0R) COPPER (UNII: 789U1901C5) PENICILLOYL POLYLYSINE (UNII: RKH8WR95Z0) THEANINE (UNII: 8021PR16QO) PASSIFLORA CAERULEA FRUIT (UNII: 15H40G5NSR) ZINC OXIDE (UNII: SOI2LOH54Z) PYRIDOXINE (UNII: KV2JZ1BI6Z) APIGENIN (UNII: 7V515PI7F6) .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) HYALURONIC ACID (UNII: S270N0TRQY) MELATONIN (UNII: JL5DK93RCL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83739-004-01 60 in 1 BOTTLE; Type 0: Not a Combination Product 10/14/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/14/2023 Labeler - XIAN CHIANG COMPANY LIMITED (662722809) Establishment Name Address ID/FEI Business Operations XIAN CHIANG COMPANY LIMITED 662722809 manufacture(83739-004)