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Throat Relief Pops by Meijer Corporation

Dosage form: lozenge
Ingredients: PECTIN 10mg
Labeler: Meijer Corporation
NDC Code: 41250-145

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Pectin 10 mg

Active ingredient (in each pop)

Pectin 10mg


Oral demulcent


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


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.


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 and zinc gluconate.

Other information:

Not a candy

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

pectin lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-145
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
Colorpurple (Purple and Red) Scoreno score
FlavorGRAPE (Grape and Cherry) Imprint Code
#Item CodePackage Description
1NDC:41250-145-2020 LOZENGE in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35604/10/2017
Labeler - Meijer Corporation (006959555)
Registrant - Bestco Inc. (002149136)
Bestco Inc.002149136manufacture(41250-145)

Meijer Corporation

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Medically reviewed on Apr 18, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.