Label: EXOSCRT SCALP CARE HRLV- biotin powder
- NDC Code(s): 72951-130-01, 72951-130-02
- 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
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENTS
Rosa Damascena Callus Extracellular Vesicles, Trehalose, Mannitol, Methionine, Glutamine, Sodium Bicarbonate, Potassium Chloride, Alanine, Arginine, Lysine HCL, Tryptophan, Tyrosine, Valine, Histidine, Aspartic Acid, Glutamic Acid, Nicotinamide Adenine Dinucleotide, Disodium Flavine Adenine Dinucleotide, Thiamine Diphosphate, Coenzyme A, sh-Oligopeptide-1, sh-Oligopeptide-4, sh-Polypeptide-4, sh-Polypeptide-9, sh-Polypeptide-13, sh-Polypeptide-8, sh-Polypeptide-1, sh-Polypeptide-3, sh-Oligopeptide-2, sh-Polypeptide-11, Copper Tripeptide-1, Leucine, Isoleucine, Phenylalanine, Glycine, Serine, Ornithine HCL, Threonine, Magnesium Sulfate, Proline, Ascorbic Acid
- 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 SCALP CARE HRLV
biotin powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72951-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Biotin (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) Biotin 0.01 mg in 20 mg Inactive Ingredients Ingredient Name Strength Trehalose (UNII: B8WCK70T7I) Mannitol (UNII: 3OWL53L36A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72951-130-02 5 in 1 CARTON 10/01/2021 1 NDC:72951-130-01 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 Labeler - Exocobio Inc. (694828578) Registrant - Exocobio Inc. (694828578) Establishment Name Address ID/FEI Business Operations Exocobio Inc. 694828578 manufacture(72951-130)