GUNA THROAT AND GUMS

Manufacturer
Guna spa
Effective date
2021-02-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:23

Label at a glance#

ProductGUNA THROAT AND GUMS
Active ingredientACONITUM NAPELLUS, ARNICA MONTANA, ATROPA BELLADONNA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, WITCH HAZEL, CALCIUM SULFIDE, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, COMFREY ROOT
Label structure10 sections

Indications and uses

Relieves symptoms of inflammation of throat, gums and oral cavity, such as: pain hoarseness swollen tonsils toothache

Dosage and administration

Adults and children 12 years and older 2 sprays, 3-5 times per day Children between 12 and 6 years of age 1 spray, 3-5 times per day Children under 6 years consult a physician

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Inactive ingredients: Ethyl alcohol 20 %, pine essential oil, lemon essential oil, polysorbate-80.

INDICATIONS & USAGE SECTION

Directions: Rotate the sprayer to the upright position. Spray as needed onto affected areas: mouth, throat, or gums.

QUESTIONS

OTC - QUESTIONS SECTION

Questions?: info@gunainc.com

(484) 223-3500


DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older 2 sprays, 3-5 times per day



Children between 12 and 6 years of age 1 spray, 3-5 times per day



Children under 6 years consult a physician




WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

WARNINGS

WARNINGS SECTION

  • Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a health professional promptly. ●Stop use and ask doctor if symptoms persist more than 3 days. ● If pregnant or breast-feeding ask a health care professional before use.● Keep out of reach of children. In case of overdose, get medical seek professional assistance or contact a Poison Control Center immediately. ● Contains ethyl alcohol 20%

USES

OTC - PURPOSE SECTION

Relieves symptoms of inflammation of throat, gums and oral cavity, such as:

  • pain
  • hoarseness
  • swollen tonsils
  • toothache

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Aconitum napellus 3X

Arnica montana 3X

Belladonna 4X

Echinacea 2X

Echinacea purpurea 2X

Hamamelis virginiana 2X

Hepar sulphuris calcareum 6X

Hypericum perforatum 3X

Millefolium 3X

Symphytum officinale 6X

RELIEF OF INFLAMMATION AND PAIN

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USTEG-45USTEG-4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USTEG5USTEG-4.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-479-27GUNA THROAT AND GUMS1 in 1 BOXSPRAY11
17089-479-27GUNA THROAT AND GUMS50 mL in 1 BOTTLE, SPRAYSPRAY501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-479GUNA THROAT AND GUMS (ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL -) SPRAY [GUNA SPA]1Current NDC, Legacy NDC, 2 package rows20210217_ba484531-ef7a-17ed-e053-2995a90a50b3.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-47917089-479-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GUNA THROAT AND GUMSACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - WITCH HAZEL -Guna spaba484531-ef7a-17ed-e053-2995a90a50b32021-02-17WarningsExact identifier
ndc (package): 17089-479-27
ndc (product): 17089-479
ndc11 (package): 17089047927
spl id: ba483fd7-f25d-cc95-e053-2995a90afd8a
spl set id: ba484531-ef7a-17ed-e053-2995a90a50b3

Reported adverse events (FAERS/openFDA)#

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