HALLS CHERRY- menthol lozenge 
Mondelez Global LLC

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HALLS CHERRY bag

Active Ingredient

<(per drop) Menthol 5.8 mg>

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 by fever, headache, rash, swelling, or vomiting, consult a doctor promptly. These may be serious.>

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children

Enter section text here

Directions

Other information

Inactive ingredients

<eucalyptus oil, FDC blue 2, FDC red 40, flavors, glucose syrup, soy lecithin, sucralose, sucrose, water>

Questions

<Call 1-800-524-2854, Monday to Friday, 9AM-6PM Eastern Time or visit our website at www.gethalls.com>

OTC Principal Display Panel

NDC 12546-109-30 Halls Cherry 30ct

HALLS  CHERRY
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12546-109
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5.8 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
WATER (UNII: 059QF0KO0R)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
Colorred (RED) Scoreno score
ShapeOVALSize21mm
FlavorCHERRY (CHERRY) Imprint Code H
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12546-109-1818 in 1 BAG; Type 0: Not a Combination Product03/31/201909/19/2022
2NDC:12546-109-3030 in 1 BAG; Type 0: Not a Combination Product03/31/2019
3NDC:12546-109-2424 in 1 BAG; Type 0: Not a Combination Product12/02/201906/11/2023
4NDC:12546-109-4040 in 1 BAG; Type 0: Not a Combination Product03/31/201908/21/2023
5NDC:12546-109-8080 in 1 BAG; Type 0: Not a Combination Product03/31/2019
6NDC:12546-109-89200 in 1 BAG; Type 0: Not a Combination Product03/31/2019
7NDC:12546-109-1616 in 1 BAG; Type 0: Not a Combination Product03/31/201912/31/2020
8NDC:12546-109-9696 in 1 BAG; Type 0: Not a Combination Product03/31/201904/21/2020
9NDC:12546-109-1414 in 1 BAG; Type 0: Not a Combination Product03/31/2019
10NDC:12546-109-99160 in 1 PACKAGE; Type 0: Not a Combination Product03/31/2019
11NDC:12546-109-01100000 in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product12/02/201909/16/2022
12NDC:12546-109-02150000 in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product12/02/201909/16/2022
13NDC:12546-109-032400 in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product12/02/201909/16/2022
14NDC:12546-109-04720 in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product12/02/201909/16/2022
15NDC:12546-109-00140 in 1 BAG; Type 0: Not a Combination Product04/10/2023
16NDC:12546-109-90250 in 1 JAR; Type 0: Not a Combination Product05/20/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/31/2019
Labeler - Mondelez Global LLC (091849786)
Establishment
NameAddressID/FEIBusiness Operations
Mondelez Canada Inc.246791201manufacture(12546-109)

Revised: 5/2024
Document Id: 187ecc1b-cd27-7253-e063-6294a90a0565
Set id: 5f4af8e8-8550-45c7-a199-694efac9e7be
Version: 17
Effective Time: 20240515
 
Mondelez Global LLC