THROAT RELIEF POPS- pectin lozenge 
Meijer Corporation

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Pectin 10 mg

Active ingredient (in each pop)

Pectin 10mg

Purpose

Oral demulcent

Uses

For temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat.

Warnings

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.

Stop use and ask doctor if

  • irritation, pain or redness persists or worsens
  • sore mouth does not improve in 7 days

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

Keep out of reach of children.

Directions

adults and children 3 years and over - allow 1 pop to dissolve slowly in mouth. May be repeated as necessary or as directed by a doctor.

children under 3 years - ask a doctor

Inactive ingredients: Ascorbic acid, citric acid, corn starch, corn syrup, FD&C Blue #1, FD&C Red #40, glycerin, medium chain triglycerides, natural and artificial flavors, sodium ascorbate, soybean oil, sucrose, water and zinc gluconate.

Other information:

Not a candy

Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST

Meijer Throat Pop 20ct

THROAT RELIEF POPS 
pectin lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-145
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PECTIN (UNII: 89NA02M4RX) (PECTIN - UNII:89NA02M4RX) PECTIN10 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorpurple (Purple and Red) Scoreno score
ShapeROUNDSize20mm
FlavorGRAPE (Grape and Cherry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41250-145-2020 in 1 BAG; Type 0: Not a Combination Product04/10/2017
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/10/201711/01/2023
Labeler - Meijer Corporation (006959555)
Registrant - Bestco Inc. (002149136)
Establishment
NameAddressID/FEIBusiness Operations
Bestco Inc.002149136manufacture(41250-145)

Revised: 10/2023
 
Meijer Corporation