EXOSCRT DERMA SIGNAL SRLV VIAL 2. DILUENT- leucine, isoleucine liquid

ExoSCRT Derma Signal SRLV Vial 2. Diluent by

Drug Labeling and Warnings

ExoSCRT Derma Signal SRLV Vial 2. Diluent by is a Otc medication manufactured, distributed, or labeled by Exocobio Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Leucine 0.05%
Isoleucine 0.05%

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

Anti wrinkle

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

KEEP OUT OF REACH OF CHILDREN

Uses

■ Helps improve wrinkle care, skin rejuvenation.

Directions

■ Mix Vial 1(Lyophilized Powder) and Vial 2(Diluent) thoroughly.
Apply a proper amount of mixture around the facial area.
* One time use ONLY.

Other Information

Store at 2℃~8℃

Questions

www.exocobio.com / sales@exocobio.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXOSCRT DERMA SIGNAL SRLV VIAL 2. DILUENT 
leucine, isoleucine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72951-150
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 mL
ISOLEUCINE (UNII: 04Y7590D77) (ISOLEUCINE - UNII:04Y7590D77)	ISOLEUCINE	0.0025 g  in 5 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	NDC: 72951-150-02	5 in 1 CARTON	10/01/2021
1	NDC: 72951-150-01	5 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

Labeler - Exocobio Inc. (694828578)

Registrant - Exocobio Inc. (694828578)

Establishment
Name	Address	ID/FEI	Business Operations
Exocobio Inc.		694828578	manufacture(72951-150)