Label: EXOSCRT DERMA SIGNAL KIT SRLV- leucine, isoleucine kit
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Contains inactivated NDC Code(s)
NDC Code(s): 72951-110-01 - Packager: Exocobio Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 23, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
[ExoSCRT Derma Signal SRLV Vial 1. Lyophilized Powder]
Inactive ingredients
Rosa Damascena Callus Extracellular Vesicles, Methionine, Trehalose, Mannitol, Glutamine, Potassium Chloride, Ascorbic Acid, Retinol, Magnesium Sulfate, Glutathione, Nicotinamide Adenine Dinucleotide, Disodium Flavine Adenine Dinucleotide, Thiamine Diphosphate, Coenzyme A, sh-Oligopeptide-2, Acetyl Hexapeptide-8, Nonapeptide-1, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, sh-Oligopeptide-1, sh-Polypeptide-1, sh-Polypeptide-3, sh-Polypeptide-76, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, Alanine, Arginine, Aspartic Acid, Glutamic Acid, Glycine, Histidine, Lysine HCL, Ornithine HCL, Phenylalanine, Proline, Serine, Threonine, Tryptophan, Tyrosine, Valine[ExoSCRT Derma Signal SRLV Vial 2. Diluent]
Inactive ingredients
Water, Sodium Hyaluronate, Sodium Chloride, Sodium Bicarbonate, Disodium Phosphate, Sodium Phosphate, Potassium Chloride, Alanine, Arginine, Histidine, Lysine HCL, Phenylalanine, Proline, Serine, Threonine, Valine, sh-Decapeptide-7, sh-Octapeptide-4, sh-Oligopeptide-9, sh-Pentapeptide-5 - PURPOSE
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WARNINGS
For external use only, not to be swallowed.
In case of accidental ingestion, seek professional assistance.
Avoid contact with eyes.
If contact occurs, rinse eyes thoroughly with water.
Stop using and consult a doctor if rash or irritation develops and lasts. Keep out of reach of children. Take proper precautions when opening. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other Information
- Questions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EXOSCRT DERMA SIGNAL KIT SRLV
leucine, isoleucine kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72951-110 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72951-110-01 1 in 1 CARTON; Type 0: Not a Combination Product 10/01/2021 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 VIAL 20 mg Part 2 1 VIAL 5.0 mL Part 1 of 2 EXOSCRT DERMA SIGNAL SRLV VIAL 1. LYOPHILIZED
leucine, isoleucine powderProduct Information Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Leucine (UNII: GMW67QNF9C) (LEUCINE - UNII:GMW67QNF9C) Leucine 0.01 mg in 20 mg Isoleucine (UNII: 04Y7590D77) (ISOLEUCINE - UNII:04Y7590D77) Isoleucine 0.01 mg in 20 mg Inactive Ingredients Ingredient Name Strength Methionine (UNII: AE28F7PNPL) Mannitol (UNII: 3OWL53L36A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 20 mg in 1 VIAL; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2021 Part 2 of 2 EXOSCRT DERMA SIGNAL SRLV VIAL 2. DILUENT
leucine, isoleucine liquidProduct Information Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Leucine (UNII: GMW67QNF9C) (LEUCINE - UNII:GMW67QNF9C) Leucine 0.0025 g in 5.0 mL Isoleucine (UNII: 04Y7590D77) (ISOLEUCINE - UNII:04Y7590D77) Isoleucine 0.0025 g in 5.0 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 5.0 mL in 1 VIAL; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2021 Labeler - Exocobio Inc. (694828578) Registrant - Exocobio Inc. (694828578) Establishment Name Address ID/FEI Business Operations Exocobio Inc. 694828578 manufacture(72951-110)