Label: K2LTS BRAIN RHABILITATION- brain rhabilitation liquid
- NDC Code(s): 84429-001-01
- Packager: K2LT LAB, LLC
- 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 June 20, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
K2LTS BRAIN RHABILITATION
brain rhabilitation liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84429-001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 23 g in 100 Inactive Ingredients Ingredient Name Strength ERGOTHIONEINE (UNII: BDZ3DQM98W) PYRIDOXINE (UNII: KV2JZ1BI6Z) PHOSPHATIDYL SERINE (UNII: 394XK0IH40) RHOPILEMA JELLYFISH (UNII: 7G5518UYJH) THREONINE (UNII: 2ZD004190S) SPERMIDINE (UNII: U87FK77H25) UROLITHIN A (UNII: ILJ8NEF6DT) CYANOCOBALAMIN (UNII: P6YC3EG204) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84429-001-01 20 in 1 BOX; Type 0: Not a Combination Product 06/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/20/2024 Labeler - K2LT LAB, LLC (072189878) Establishment Name Address ID/FEI Business Operations K2LT LAB, LLC 072189878 manufacture(84429-001)