Plantain Spruce Cough by Uriel Pharmacy Inc Plantain Spruce Cough

Plantain Spruce Cough by

Drug Labeling and Warnings

Plantain Spruce Cough by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PLANTAIN SPRUCE COUGH- plantain spruce cough syrup 
Uriel Pharmacy Inc

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Plantain Spruce Cough

Directions: FOR ORAL USE ONLY.

Take up to every hour as needed. Ages 12 and older: 1 tablespoon. Ages 2-11: 1 teaspoon. Under age 2: Consult a doctor.

Active Ingredients: 100 gm contains: 30 gm Plantago (Ribwort plantain) 1X, 15 gm Picea abies (Spruce) 1X, 2.5 gm Petasites (Butterbur) 1X, 2.5 gm Prunus (Blackthorn) 1X; Drosera (Sundew) 4X, Atropa belladonna (Nightshade) 5X, China (Peruvian bark) 5X, Coccus cacti (Cochineal bug, female) 5X, Helleborus (Christmas rose) 5X, |pecacuanha (Ipecac) 5X, Mephitis (Secretion from the rectal gland of skunk) 7X, Veratrum (White hellebore) 5X

Inactive Ingredients: Distilled water, Organic cane sugar, Wild cherry flavor, Beet Root Powder, Organic vanilla extract, Citric acid

Uses: Temporary relief of cough and chest congestion.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PLANTAIN SPRUCE COUGH 
plantain spruce cough syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-8388
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLANTAGO LANCEOLATA WHOLE (UNII: TJ55Y9N2M4) (PLANTAGO LANCEOLATA WHOLE - UNII:TJ55Y9N2M4)	PLANTAGO LANCEOLATA WHOLE	1 [hp_X]  in 1 mL
IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L)	IPECAC	5 [hp_X]  in 1 mL
PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT)	PROTORTONIA CACTI	5 [hp_X]  in 1 mL
HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815)	HELLEBORUS NIGER ROOT	5 [hp_X]  in 1 mL
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	4 [hp_X]  in 1 mL
MEPHITIS MEPHITIS ANAL GLAND FLUID (UNII: 3BN57UN4US) (MEPHITIS MEPHITIS ANAL GLAND FLUID - UNII:3BN57UN4US)	MEPHITIS MEPHITIS ANAL GLAND FLUID	7 [hp_X]  in 1 mL
VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z)	VERATRUM ALBUM ROOT	5 [hp_X]  in 1 mL
CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB)	CINCHONA OFFICINALIS BARK	5 [hp_X]  in 1 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	5 [hp_X]  in 1 mL
PICEA ABIES WHOLE (UNII: D77PG8S4KK) (PICEA ABIES WHOLE - UNII:D77PG8S4KK)	PICEA ABIES WHOLE	1 [hp_X]  in 1 mL
PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R)	PETASITES HYBRIDUS ROOT	1 [hp_X]  in 1 mL
SLOE (UNII: 3MLB4858X7) (SLOE - UNII:3MLB4858X7)	SLOE	1 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BEET TOP (UNII: YB1P778Q1C)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)
SWEET CHERRY JUICE (UNII: 7019G1D33H)
VANILLA (UNII: Q74T35078H)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-8388-1	125 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009	01/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009	01/11/2022

Labeler - Uriel Pharmacy Inc (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc		043471163	manufacture(48951-8388)

Revised: 1/2022

Document Id: d6a7e75d-3b4d-10bf-e053-2995a90a2cc2

34390-5

Set id: d437c077-5bb1-7a69-e053-2a95a90ab0da

Version: 2

Effective Time: 20220128