SF MENTHOL COUGH DROP- menthol lozenge 
United Natural Foods, Inc. dba UNFI

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Menthol 5.8 mg

Active ingredient (in each drop)

Menthol 5.8mg

Purposes

Cough suppressant / Oral anesthetic

Uses temporarily relieves:

Warnings

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headaches, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

Ask a doctor before use if you have:

Stop use and consult doctor if

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

Keep out of reach of children.

Directions

Adults and children 5 years and over - dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.

Children under 5 years - ask a doctor

Other information

Inactive Ingredients: Acesulfame potassium, corn starch, eucalyptus oil, FD&C blue no 1, FD&C red no. 40, glycerin, gum arabic, isomalt, maltitol syrup, medium chain triglycerides, natural and artificial flavors, potassium sorbate, soybean oil, sucralose and water.

Questions? Or to report an adverse event call 1-877-932-7948.

Equaline SF Menthol 25ct Cough Drops

SF MENTHOL COUGH DROP 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-027
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5.8 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorblue (Light blue with flakes) Scorescore with uneven pieces
ShapeOVALSize16mm
FlavorMENTHOLImprint Code B
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-027-2525 in 1 BAG; Type 0: Not a Combination Product06/18/2014
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/18/2014
Labeler - United Natural Foods, Inc. dba UNFI (943556183)
Registrant - Bestco, Inc (002149136)
Establishment
NameAddressID/FEIBusiness Operations
Bestco, Inc002149136manufacture(41163-027)

Revised: 1/2024
Document Id: 0f1702d1-8250-2614-e063-6394a90aafe6
Set id: 46c466d7-26ca-5179-e054-00144ff88e88
Version: 6
Effective Time: 20240116
 
United Natural Foods, Inc. dba UNFI