Original Extra Strong All Natural Fishermans Friend Menthol Cough Suppressant

Manufacturer
Lofthouse of Fleetwood, Ltd.
Effective date
2021-05-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:40:22

Label at a glance#

ProductOriginal Extra Strong All Natural Fishermans Friend Menthol Cough Suppressant
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

temporarily relieves cough due to minor throat and bronchial irritation occurring with the common cold or inhaled irritants occasional minor sore throat

Dosage and administration

adults and children 2 years of age and over: allow 1 lozenge to dissolve slowly in the mouth repeat every 2 hours as needed or as directed by a doctor children under 2 years of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredient (in each lozenge)

OTC - ACTIVE INGREDIENT SECTION

Menthol 10 mg

Purpose

OTC - PURPOSE SECTION

Cough suppressant/oral anesthetic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves

  • cough due to minor throat and bronchial irritation occurring with the common cold or inhaled irritants
  • occasional minor sore throat

Warnings

WARNINGS SECTION

Sore throat warning: Severe or persistent sore throat or sore throat that occurs with high fever, headache, nausea, and vomitting may be serious. Ask a doctor right away. Do not use more than 2 days or give to children under 2 years of age unless directed by a doctor.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • cough that occurs with too much phlegm (mucus)
  • a persistent or chronic cough that lasts such as occurs with smoking, asthma, or emphysema

OTC - WHEN USING SECTION

When using this product

do not use more than directed

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.
  • sore throat is severe, lasts more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding

ask a health care professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and over: allow 1 lozenge to dissolve slowly in the mouth
  • repeat every 2 hours as needed or as directed by a doctor
  • children under 2 years of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

capsicum, dextrin, eucalyptus oil, natural licorice, sugar, tragacanth

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FISHERMAN'S FRIEND ®

ORIGINAL EXTRA STRONG

Menthol Cough Suppressant Lozenges

Cough Suppressant/Oral Anesthetic

38 Lozenges

Manufactured by: Lofthouse of Fleetwood Ltd., Fleetwood, Lancs, England

Distributed by: Greenwood Brands, LLC.

Buffalo-Niagara, NY 14225

ffinfo@greenwoodg.com

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014609Fisherman's Friend 10 MG Oral LozengePSN3
199393menthol 10 MG Oral LozengePSN3
1014609menthol 10 MG Oral Lozenge [Fisherman's Friend]SBD3
199393menthol 10 MG Oral LozengeSCD3
1014609Fisherman's Friend 10 MG Oral LozengeSY3
199393menthol 10 MG Oral PastilleSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55711-064-02Original Extra Strong All Natural Fishermans Friend Menthol Cough Suppressant38 in 1 BOXLOZENGE383

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55711-064ORIGINAL EXTRA STRONG ALL NATURAL FISHERMANS FRIEND MENTHOL COUGH SUPPRESSANT (MENTHOL) LOZENGE [LOFTHOUSE OF FLEETWOOD, LTD.]3Current NDC, Legacy NDC, 1 package rows20210515_acbcbc4e-e0dc-45ba-9323-680d4004adea.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MentholACTIVE INGREDIENTL7T10EIP3A1
MentholACTIVE MOIETYL7T10EIP3A1
CapsicumINACTIVE INGREDIENT00UK7646FG1
Eucalyptus OilINACTIVE INGREDIENT2R04ONI6621
LicoriceINACTIVE INGREDIENT61ZBX548831
Raw SugarINACTIVE INGREDIENT8M707QY5GH1
TragacanthINACTIVE INGREDIENT2944357O2O1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55711-06455711-064-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 18 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
TragacanthTRAGACANTH2944357O2OTABLET / ORAL12 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, EXTENDED RELEASE / ORAL7 mgExact identifier — unii+route
16 equally ranked IID candidates
Eucalyptus OilEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii+route
2 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, COATED / ORAL7.5 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OSUSPENSION, EXTENDED RELEASE / ORAL70 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OWAFER / ORAL32 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OPOWDER, FOR SUSPENSION / ORAL60 mg/1mlExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OWAFER / ORAL32 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, EXTENDED RELEASE / ORAL7 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OSUSPENSION, EXTENDED RELEASE / ORAL70 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET, COATED / ORAL7.5 mgExact identifier — unii+route
16 equally ranked IID candidates
Eucalyptus OilEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii+route
2 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OSUSPENSION / ORAL130 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OTABLET / ORAL12 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OSUSPENSION / ORAL130 mgExact identifier — unii+route
16 equally ranked IID candidates
TragacanthTRAGACANTH2944357O2OPOWDER, FOR SUSPENSION / ORAL60 mg/1mlExact identifier — unii+route
16 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Original Extra Strong All Natural Fishermans Friend Menthol Cough SuppressantMENTHOLLofthouse of Fleetwood, Ltd.d8f4a65b-cf2c-4424-b27f-e3e0ffadd9cf2025-09-30WarningsExact identifier
ndc (package): 55711-064-02
ndc (product): 55711-064
ndc11 (package): 55711006402
c238726c-d28b-4157-e053-2995a90adc96acbcbc4e-e0dc-45ba-9323-680d4004adea2021-05-13WarningsExact identifier
spl id: c238726c-d28b-4157-e053-2995a90adc96
spl set id: acbcbc4e-e0dc-45ba-9323-680d4004adea

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.