PETASITES PLANTAGO SPECIAL ORDER- petasites plantago special order liquid
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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Petasites Plantago Special Order

Directions: FOR ORAL USE.

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredients: Abies e summ. 3X, Petasites e rad. 3X, Plantago e fol. 3X, Vivianite 8X, Pulmo 17X

Inactive Ingredients: Water, Salt

Use: Temporary relief of cough.

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.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

PetasitesPlantagoSpecialOrderAmpules

PETASITES PLANTAGO SPECIAL ORDER
petasites plantago special order liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-8019
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ABIES ALBA LEAFY TWIG (UNII: CE3G3J56LR) (ABIES ALBA LEAFY TWIG - UNII:CE3G3J56LR)	ABIES ALBA LEAFY TWIG	3 [hp_X] in 1 mL
PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R)	PETASITES HYBRIDUS ROOT	3 [hp_X] in 1 mL
PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X)	PLANTAGO MAJOR LEAF	3 [hp_X] in 1 mL
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7)	FERROSOFERRIC PHOSPHATE	8 [hp_X] in 1 mL
SUS SCROFA LUNG (UNII: 7GL3G1COB3) (SUS SCROFA LUNG - UNII:7GL3G1COB3)	SUS SCROFA LUNG	7 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-8019-1	10 in 1 BOX	09/01/2009	10/09/2020
1		1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	10/09/2020

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-8019)

Revised: 6/2021

Document Id: c55c4336-c23d-c513-e053-2995a90a2070

Set id: 48654e04-b83b-405f-8e88-1056826d17f7

Version: 3

Effective Time: 20210622

Uriel Pharmacy Inc.