NATURAL RELIEF COUGH AND CONGESTION COUGH AND CONGESTION SYMPTOM RELIEF- antimonium tartaricum, coccus cacti, cuprum metallicum, drosera rotundifolia, echinacea angustifolia, kali carbonicum, mephitis mephitica, natrum muriaticum, rumex crispus, zincum gluconicum spray

Natural Relief Cough and Congestion by

Drug Labeling and Warnings

Natural Relief Cough and Congestion by is a Homeopathic medication manufactured, distributed, or labeled by TRP Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Antimonium tartaricum HPUS 6C, 12C, 18C;

Coccus cacti HPUS 6C, 12C,18C;

Cuprum metallicum HPUS 6C, 12C,18C;

Drosera (rotundifolia) HPUS 6C, 12C, 18C;

Echinacea (angustifolia) HPUS 6C, 12C, 18C;

Kali carbonicum HPUS 6C, 12C,18C;

Mephitis mephitica HPUS 12C, 18C;

Natrum muriaticum HPUS 6X, 12X,30X;

Rumex crispus HPUS 6C, 12C, 18C;

Zincum gluconicum HPUS 4X, 6X

USES:

According to homeopathic indications, these ingredients provide temporary relief from symptoms of cough and congestion.

*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur. This product is intended to be taken orally. Do not use in eyes or nose.

When using

When using this product avoid contact with the eyes.

Rinse right away with water if the product gets in your eye.

KEEP OUT OF REACH OF CHILDREN:

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

Pregnancy warning

If pregnant or breast-feeding, ask a health professional before use.

DIRECTIONS:

Suitable for adults and children ages 12 and over.
Spray 2-3 times in mouth. Keep in mouth for 15 seconds before swallowing. Use up to 6 times a day as needed. Use at least 10 minutes before or at least 10 minutes after eating or drinking.

Children under the age of 12: Consult a physician before use.

INDICATIONS:

Uses*

According to homeopathic indications, these ingredients provide temporary relief from symptoms of cough and congestion.. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Stop use

Stop use and ask a doctor if: Symptoms last longer than 7 days.

INACTIVE INGREDIENTS:

Alcohol 25%, Demineralized water, Fruit juice concentrates, Invert sugar, Natural flavor, Propylene glycol, Sodium bicarbonate.

Other information

Other information

Homeopathic remedies may not be effective for everyone. Individual results may vary.

Replace cap after each use.
Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications.
Cough & Congestion Spray TM is a homeopathic dilution, for details see www.thereliefproducts.com.

QUESTIONS:

Questions or comments

1-888-969-6855

8 am to 4 pm EST;

Monday - Friday

www.thereliefproducts.com

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

NATURAL RELIEF COUGH AND CONGESTION  COUGH AND CONGESTION SYMPTOM RELIEF
antimonium tartaricum, coccus cacti, cuprum metallicum, drosera rotundifolia, echinacea angustifolia, kali carbonicum, mephitis mephitica, natrum muriaticum, rumex crispus, zincum gluconicum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17312-432
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_C]  in 1 mL
ZINC GLUCONATE (UNII: U6WSN5SQ1Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC GLUCONATE	4 [hp_X]  in 1 mL
RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C)	RUMEX CRISPUS ROOT	6 [hp_C]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	6 [hp_X]  in 1 mL
MEPHITIS MEPHITIS ANAL GLAND FLUID (UNII: 3BN57UN4US) (MEPHITIS MEPHITIS ANAL GLAND FLUID - UNII:3BN57UN4US)	MEPHITIS MEPHITIS ANAL GLAND FLUID	12 [hp_C]  in 1 mL
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	6 [hp_C]  in 1 mL
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8)	ECHINACEA ANGUSTIFOLIA	6 [hp_C]  in 1 mL
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	6 [hp_C]  in 1 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	6 [hp_C]  in 1 mL
PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT)	PROTORTONIA CACTI	6 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
INVERT SUGAR (UNII: ED959S6ACY)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17312-432-23	1 in 1 CARTON	08/06/2024
1		20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/06/2024

Labeler - TRP Company (105185719)