ARTEMIC RESCUE- oral spray spray, suspension

ArtemiC Rescue by

Drug Labeling and Warnings

ArtemiC Rescue by is a Otc medication manufactured, distributed, or labeled by AMC Pharma LLC, Kinezika d.o.o.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

Water-based suspension, dietary supplement Oral Spray

ACTIVE INGREDIENT

Curcuma Longa Extract, Boswellia SerrataExtract, Antioxidant Artemisinin,Vitamin C (L-Ascorbic Acid)

INACTIVE INGREDIENT

Water, Vegetable Castor Oil, Natural Propanediol, DL-Alpha-Tocopherol

DOSAGE & ADMINISTRATION

5 sprays provides 1 ml of ArtemiC. Servings per container: 4

INSTRUCTIONS FOR USE

Shake well before using. Adults apply 5 sprays, twice daily in the mouth, morning and evening for 2 consecutive days.preferably at least half hour before eating.

WARNINGS

Keep out of reach of children. Not intended for pregnant or nursing woman. Discontinue use or consult your doctor if any adverse reactions occur. Do not use if inner bottle or spray cap is broken, or shows sign of tampering.

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children.

STORAGE AND HANDLING

Store in a dry, cool place and avoid heat and direct sunlight. Do not exceed temperatures above 77 deg F. Usable until expiration date. Once opened, use witjin 1 month. Do not freeze.

INDICATIONS & USAGE

Adults apply 5 sprays, twice daily, into mouth.

PURPOSE

Dietary supplement to support the immune system.

PRINCIPAL DISPLAY PANEL

NDC: 83278-001-05

Bottle label NDC: 83278-001-05

INGREDIENTS AND APPEARANCE

ARTEMIC RESCUE 
oral spray spray, suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83278-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISININ (UNII: 9RMU91N5K2) (ARTEMISININ - UNII:9RMU91N5K2)	ARTEMISININ	0.6 g  in 100 g
CURCUMIN (UNII: IT942ZTH98) (CURCUMIN - UNII:IT942ZTH98)	CURCUMIN	2 g  in 100 g
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	6 g  in 100 g
BOSWELLIA SACRA BARK (UNII: 1UK28DX728) (BOSWELLIA SACRA BARK - UNII:1UK28DX728)	BOSWELLIA SACRA BARK	1.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)	0.3 g  in 100 g
WATER (UNII: 059QF0KO0R)	89 g  in 100 g
PROPANEDIOL (UNII: 5965N8W85T)	0.3 g  in 100 g
CASTOR OIL (UNII: D5340Y2I9G)	0.3 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83278-001-05	5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/20/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/20/2023

Labeler - AMC Pharma LLC (118750577)

Registrant - AMC Pharma LLC (118750577)

Establishment
Name	Address	ID/FEI	Business Operations
Kinezika d.o.o.		500690887	manufacture(83278-001)