Plantago primula pellet

Indications & usage section

Directions: FOR ORAL USE ONLY.

Dosage & administration section

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.

Otc - active ingredient section

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

Inactive ingredient section

Inactive Ingredient: Organic sucrose

Otc - purpose section

Use: Temporary relief of headache.

Otc - keep out of reach of children section


Warnings section

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.

Otc - questions section

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120

Ingredients and appearance - Product information

Plantago primula pellet- Plantago primula

Product information

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

Active Ingredient/Active Moiety

Ingredient Name Strength
Plantago major leaf ( UNII: 7DC28K241X)( Plantago major leaf - UNII: 7DC28K241X ) 1 [hp_X]in 1
Primula veris flower ( UNII: W5BET37294)( Primula veris flower - UNII: W5BET37294 ) 1 [hp_X]in 1
Hyoscyamus niger leaf ( UNII: 32IT7G8BAW)( Hyoscyamus niger leaf - UNII: 32IT7G8BAW ) 4 [hp_X]in 1

Inactive Ingredients

Ingredient Name Code
Sucrose ( UNII: C151H8M554)

Product Characteristics

Color white Shape ROUND
Size 3 mm Score 1


# Item Code Package Description Marketing Start Date
1 NDC: 48951-8035-2 1350 in 1 BOTTLE, GLASS 2009/09/01

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
unapproved homeopathic USA 2009/09/01

Labeler - Uriel Pharmacy Inc.( 043471163)


Name ID/FEI Business Operations
Uriel Pharmacy Inc. 043471163 manufacture( 48951-8035)

Package label.principal display panel