PLANTAGO PRIMULA- plantago primula pellet
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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Plantago Primula

Directions: FOR ORAL USE ONLY.

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

Active Ingredients: 100 gm contains: 2.5 gm Plantago (Ribwort plantain) 1X, 2.5 gm Primula (Cowslip) 1X; Hyoscyamus (Henbane) 4X

Inactive Ingredient: Organic sucrose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if condtions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

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

PlantagoPrimulaPellets

PLANTAGO PRIMULA
plantago primula pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-8035
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X)	PLANTAGO MAJOR LEAF	1 [hp_X]
PRIMULA VERIS FLOWER (UNII: W5BET37294) (PRIMULA VERIS FLOWER - UNII:W5BET37294)	PRIMULA VERIS FLOWER	1 [hp_X]
HYOSCYAMUS NIGER LEAF (UNII: 32IT7G8BAW) (HYOSCYAMUS NIGER LEAF - UNII:32IT7G8BAW)	HYOSCYAMUS NIGER LEAF	4 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	3mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-8035-2	1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009	10/09/2020

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(48951-8035)

Revised: 12/2020

Document Id: b5a5f86e-ab44-8e52-e053-2995a90a80be

Set id: c6f1afea-1938-4fad-9f3f-a02fb3dc8dd6

Version: 4

Effective Time: 20201204

Uriel Pharmacy Inc.