FATHER JOHNS COUGH MEDICINE PLUS- nasal decongestant liquid

Father Johns Cough Medicine Plus by

Drug Labeling and Warnings

Father Johns Cough Medicine Plus by is a Otc medication manufactured, distributed, or labeled by Oakhurst Company, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Each 30 mL (2 tablespoonfuls) contain:

Dextromethorphan HBr, 10mg

Phenylephrine HCl, 10mg

Chlorpheniramine Maleate, 4mg

INACTIVE INGREDIENT

Citric acid

FD&C Red #40

FD&C Blue #1

Glycerin

Purified water

Sodium benzoate

Sodium chloride

Sodium citrate

Sodium saccharin

Sucrose

DOSAGE & ADMINISTRATION

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

INDICATIONS & USAGE

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

WARNINGS

WARNINGS: Do not excees recommended dosage

PURPOSE

Cough Supressant

Nasal Decongestant

Anthihistamine

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

FATHER JOHNS COUGH MEDICINE PLUS 
nasal decongestant liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 45728-445
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 30 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	10 mg  in 30 mL
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	4 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 45728-445-94	1 in 1 CARTON	06/17/2019
1		118 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	06/17/2019

Labeler - Oakhurst Company (001385111)

Registrant - Humco Holding Group, Inc (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc		825672884	label(45728-445) , pack(45728-445) , analysis(45728-445) , manufacture(45728-445)