SUCRETS SORE THROAT WILD CHERRY- dyclonine hydrochloride lozenge 
Insight Pharmaceuticals LLC

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Sucrets Sore Throat Wild Cherry

Drug Facts

Active ingredients (per lozenge)

Dyclonine hydrochloride, 2.0 mg

Purpose

Oral anesthetic

Uses

For temporary relief of occasional: 

Warnings

Sore through warning: if sore throat is severe, persists for more than 2 days, is accompanied by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly.

Stop use and ask a doctor if

  • sore mouth symptoms do not improve in 7 days
  • irritation, pain or redness persists or worsens
  • swelling, rash, or fever develops

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

corn syrup, FD&C blue no 1, FD&C red no 40, flavor, menthol, propylene glycol, sucrose, tartaric acid, water

PRINCIPAL DISPLAY PANEL

Sucrets
Dyclonine/Oral Anesthetic
Wild Cherry
18 lozenges

PRINCIPAL DISPLAY PANEL
Sucrets 
Dyclonine/Oral Anesthetic
Wild Cherry 
18 lozenges

SUCRETS SORE THROAT WILD CHERRY 
dyclonine hydrochloride lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-560
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE2 mg
Inactive Ingredients
Ingredient NameStrength
CORN SYRUP (UNII: 9G5L16BK6N)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
MENTHOL (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SUCROSE (UNII: C151H8M554)  
TARTARIC ACID (UNII: W4888I119H)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorredScoreno score
ShapeROUNDSize19mm
FlavorCHERRY (Wild Cherry) Imprint Code S
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-560-1818 in 1 CONTAINER; Type 0: Not a Combination Product07/28/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02207/28/2009
Labeler - Insight Pharmaceuticals LLC (055665422)

Revised: 3/2024
Document Id: fc445e91-7ca2-4f37-800f-efe6dffd3db1
Set id: da4967c7-ee18-42e7-8c97-8919f3bb1b7d
Version: 3
Effective Time: 20240320
 
Insight Pharmaceuticals LLC