COUGH AND MUCUS (antimonium tartaricum, euphrasia officinalis, hepar sulphuris calcareum, hydrastis canadensis, kali bichromicum, pulsatilla- pratensis, stannum metallicum, sulphur liquid

Cough and Mucus by

Drug Labeling and Warnings

Cough and Mucus by is a Homeopathic medication manufactured, distributed, or labeled by NaturalCare, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

(in each drop) Antimonium Tartaricum 6X, 12X, 30X 5.82%, Euphrasia Officinalis 6X 5.82%, Hepar Sulphuris Calcareum 12x 5.82%, Hydrastis Canadensis 5X, 30X 5.82%, Kali Bichromicum 12X, 30X 5.82%, Pulsatilla 6X 5.82%, Stannum Metallicum 12X, 30X 5.82%, Sulphur 12X 5.82%.

PURPOSE:

Antimonium Tartaricum – minor bladder irritation, Euphrasia Officinalis – runny nose, sinus pressure, Hepar Sulphuris Calcareum – cough, stubborn mucus in chest, Hydrastis Canadensis – cough with thick yellow expectoration, Kali Bichromicum – cold with thick nasal discharge, Pulsatilla – cough with yellow expectoration, Stannum Metallicum – deep productive cough triggered by mucus in the throat, Sulphur – chest congestion*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

USES:

May help temporarily relieve ■ chest congestion ■ hacking cough ■ thick mucus in chest, throat and nose*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

Do not use

■ for persistent or chronic cough such as occurs with asthma ■ if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

Stop use and ask a doctor if

■ cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash or persistent headache.

These could be signs of a serious condition

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

Do not use if tamper evident seal is missing or open.

■ Store tightly closed at room temperature (65-80ºF)

KEEP OUT OF REACH OF CHILDREN:

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

DIRECTIONS:

■ children and infants over 4 months of age place 1/2 teaspoon (2.5 ml) under the tongue every 20 min until symptoms improve, then every 4 hours as needed.

■ for children under 4 months consult a healthcare professional.

INACTIVE INGREDIENTS:

citric acid, glycerin, natural mixed berry flavor, purified water, sodium benzoate

QUESTIONS:

Dist. By NaturalCare

201 Apple Blvd.

Woodbine, IA 51579

www.NaturalCareWorks.com

1-888-280-5672

PACKAGE LABEL DISPLAY:

NaturalCare

children's

Cough & Mucus

Homeopathic

4 FL OZ (120 mL)

INGREDIENTS AND APPEARANCE

COUGH AND MUCUS 
antimonium tartaricum, euphrasia officinalis, hepar sulphuris calcareum, hydrastis canadensis, kali bichromicum, pulsatilla (pratensis), stannum metallicum, sulphur liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70163-0036
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	6 [hp_X]  in 1 mL
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	6 [hp_X]  in 1 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	12 [hp_X]  in 1 mL
GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV)	GOLDENSEAL	5 [hp_X]  in 1 mL
POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V)	POTASSIUM DICHROMATE	12 [hp_X]  in 1 mL
PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI)	PULSATILLA PRATENSIS WHOLE	6 [hp_X]  in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)	TIN	12 [hp_X]  in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	12 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Characteristics
Color		Score
Shape		Size
Flavor	BERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70163-0036-2	1 in 1 CARTON	03/23/2026
1	NDC: 70163-0036-1	120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/23/2026

Labeler - NaturalCare (078452966)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(70163-0036) , api manufacture(70163-0036) , label(70163-0036) , pack(70163-0036)