FATHER JOHNS COUGH MEDICINE PLUS- nasal decongestant liquid 
Oakhurst Company

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Father John's Medicine Plus

Each 30 mL (2 tablespoonfuls) contain:

Dextromethorphan HBr, 10mg

Phenylephrine HCl, 10mg

Chlorpheniramine Maleate, 4mg

Citric acid

FD&C Red #40

FD&C Blue #1

Glycerin

Purified water

Sodium benzoate

Sodium chloride

Sodium citrate

Sodium saccharin

Sucrose

DO NOT take more than 12 tablespoonfuls in 24 hours

Adults and Children 12 years and older: take 2 tablespoons every 4 hours

Children under 12 years old: ask a doctor

For temporarily relief of couch and allergy symptoms, including coughing, nasal congestion, and runny nose.

WARNINGS: Do not excees recommended dosage

Cough Supressant

Nasal Decongestant

Anthihistamine

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Father Johns Plus 4oz 2022fatherplus '

FATHER JOHNS COUGH MEDICINE PLUS 
nasal decongestant liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45728-445
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 30 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 30 mL
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SUCROSE (UNII: C151H8M554)  
GLYCERIN (UNII: PDC6A3C0OX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45728-445-941 in 1 CARTON06/17/2019
1118 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/17/2019
Labeler - Oakhurst Company (001385111)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114label(45728-445) , pack(45728-445) , analysis(45728-445) , manufacture(45728-445)

Revised: 12/2023
Document Id: 0ccb5970-3697-9097-e063-6294a90aa811
Set id: 8b8aab0f-251b-6bd8-e053-2995a90ad748
Version: 6
Effective Time: 20231218
 
Oakhurst Company