FDA.reportPublic FDA data

GUNA HAY FEVER RELIEF

Product NDC
17089-476
11-digit product format
170890476
Labeler code
17089
Product ID
17089-476_d3322d60-dd44-8e96-e053-2995a90a54b0
Type
HUMAN OTC DRUG
Nonproprietary name
strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -
Dosage form
PELLET
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-02-17
Substance
APIS MELLIFERA; ARSENIC TRIOXIDE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; MANGANESE; ONION; SCHOENOCAULON OFFICINALE SEED; SILVER NITRATE; STRYCHNOS NUX-VOMICA SEED; SULFUR
Active strength
200; 30; 5; 4; 200; 8; 30; 6; 6; 4; 30 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
Pharmacologic classes
Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA HAY FEVER RELIEF
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS NUX-VOMICA SEED200 [hp_X]/4g
HISTAMINE DIHYDROCHLORIDE30 [hp_X]/4g
MANGANESE5 [hp_X]/4g
SCHOENOCAULON OFFICINALE SEED4 [hp_X]/4g
ONION200 [hp_X]/4g
APIS MELLIFERA8 [hp_X]/4g
SILVER NITRATE30 [hp_X]/4g
EUPHRASIA STRICTA6 [hp_X]/4g
GALPHIMIA GLAUCA FLOWERING TOP6 [hp_X]/4g
SULFUR4 [hp_X]/4g
ARSENIC TRIOXIDE30 [hp_X]/4g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
269XH13919Internal UNII lookup
3POA0Q644UInternal UNII lookup
42Z2K6ZL8PInternal UNII lookup
6NAF1689IOInternal UNII lookup
492225Q21HInternal UNII lookup
7S82P3R43ZInternal UNII lookup
95IT3W8JZEInternal UNII lookup
C9642I91WLInternal UNII lookup
93PH5Q8M7EInternal UNII lookup
70FD1KFU70Internal UNII lookup
S7V92P67HOInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
b8db4fc6-f235-6f2b-e053-2a95a90a186fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-476-20GUNA HAY FEVER RELIEF4 g in 1 TUBEPELLET43
17089-476-20GUNA HAY FEVER RELIEF2 in 1 BOXPELLET23
17089-476-21GUNA HAY FEVER RELIEF4 g in 1 TUBEPELLET43
17089-476-21GUNA HAY FEVER RELIEF1 in 1 BOXPELLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-476GUNA HAY FEVER RELIEF (STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -) PELLET [GUNA SPA]3Current NDC, Legacy NDC, 4 package rows20211216_b8db4fc6-f235-6f2b-e053-2a95a90a186f.zip

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 HAY FEVER RELIEFSTRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -Guna spab8db4fc6-f235-6f2b-e053-2a95a90a186f2021-12-15WarningsExact identifier
ndc (product): 17089-476

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17089-476-20170890476202 TUBE in 1 BOX (17089-476-20) / 4 g in 1 TUBE2 tube2021-02-170000-00-00NoNoCurrent
17089-476-21170890476211 TUBE in 1 BOX (17089-476-21) / 4 g in 1 TUBE1 tube2021-12-150000-00-00NoNoCurrent