EPINEPHRINE PROFESSIONAL- epinephrine and isopropyl alcohol 
Focus Health Group

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Epinephrine Professional Convenience Kit

For treating anaphylaxis:

Adults and Children 30 kg (66 lbs) or more: 0.3 to 0.5 mg (0.3 to 0.5 ml) intramuscularly or subcutaneously into anterolateral aspect of the thigh every 5 to 10 minutes as necessary.

Children 30 kg (66 lbs) or less: 0.01 mg/kg (0.01 ml/kg), up to 0.3 mg (0.3 ml), intramuscularly or subcutaneously into anterolateral aspect of the thigh every 5 to 10 minutes as necessary.

Principal Display Panel

Principal Display Panel

EPINEPHRINE PROFESSIONAL 
epinephrine and isopropyl alcohol kit
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:24357-011
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24357-011-131 in 1 CARTON; Type 0: Not a Combination Product07/01/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 VIAL 1 mL
Part 24 PACKET 4 mL
Part 1 of 2
ADRENALIN 
epinephrine injection
Product Information
Item Code (Source)NDC:42023-159
Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS, INTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
TARTARIC ACID (UNII: W4888I119H) 2.25 mg  in 1 mL
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I) 1 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K) 0.2 mg  in 1 mL
SODIUM METABISULFITE (UNII: 4VON5FNS3C) 0.457 mg  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) 7.3 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42023-159-251 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA20420007/01/2013
Part 2 of 2
MCKESSON ALCOHOL PREP PAD 
isopropyl alcohol swab
Product Information
Item Code (Source)NDC:68599-5804
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68599-5804-11 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/09/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA20420007/01/2019
Labeler - Focus Health Group (826939949)
Establishment
NameAddressID/FEIBusiness Operations
Par Sterile Products LLC808402890manufacture(42023-159)
Establishment
NameAddressID/FEIBusiness Operations
Focus Health Group826939949manufacture(24357-011)

Revised: 10/2022
Document Id: eb6598c3-bb08-32e0-e053-2a95a90a13b5
Set id: 8c502fcc-1b61-7d1f-e053-2a95a90adc46
Version: 5
Effective Time: 20221019
 
Focus Health Group