Category V

Manufacturer
Vitality Works, Inc, | Vitality Works, Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:02

Label at a glance#

ProductCategory V
Active ingredientPICRIC ACID, PETROSELINUM CRISPUM, SALICYLIC ACID, SALIX NIGRA BARK, LACTIC ACID, DELPHINIUM STAPHISAGRIA SEED, URANYL NITRATE HEXAHYDRATE, HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE, AQUA REGIA, COPPER, FRAXINUS AMERICANA BARK, EPINEPHRINE, ANAGALLIS ARVENSIS, CHAMAEMELUM NOBILE, ARSENIC TRIIODIDE, CALCIUM LACTATE, ANHYDROUS CITRIC ACID, STRYCHNOS IGNATII SEED, POTASSIUM CARBONATE
Label structure8 sections

Label contents#

Full prescribing information#

Category V

OTC - ACTIVE INGREDIENT SECTION

Adrenalinum 15X                                 Fraxinus Americana 4X                       Salicylicum Acidum 9X, 12X

Anagallis Arvensis 3X                          Ignatia Amara 6X                                Salix Nigra 20X

Anthemis Nobilis 10X                           Kali Carbonicum 8X                             Sarcolacticum Acidum 10X, 15X

Arsenicum Iodatum 10X                      Murex Purpurea 14X                            Staphysagria 5X

Calcerea Lactica 14X, 50X                   Nitromuriaticum Acidum 15X                Uranium Nitricum 17X

Citricum Acidum 10X, 15X                    Petroselinum Sativum 12X, 20X

Cuprum Metallicum 15X, 25X               Picricum Acidum 12X

Category V

INACTIVE INGREDIENT SECTION

Alcohol, Purified Water

Category V

WARNINGS SECTION

Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

Category V

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Category V

INDICATIONS & USAGE SECTION

For the temporary relief of general cold and flu symptoms, fever, achiness, and cough.

Category V

DOSAGE & ADMINISTRATION SECTION

Orally 25 drops, 2 times per day or as directed by a physician. Children 12 and under use one half the adult dosage.

Category V

OTC - PURPOSE SECTION

Eases cold and flu symptoms, fever, achiness and cough.

Category V

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
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2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
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d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64616-086-02Category V59 mL in 1 BOTTLE, DROPPERLIQUID598

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANAGALLIS ARVENSISACTIVE INGREDIENT46883LR90E1
ANHYDROUS CITRIC ACIDACTIVE INGREDIENTXF417D3PSL1
AQUA REGIAACTIVE INGREDIENTX3TT5X989E1
ARSENIC TRIIODIDEACTIVE INGREDIENT3029988O2T1
CALCIUM LACTATEACTIVE INGREDIENT2URQ2N32W31
CHAMAEMELUM NOBILEACTIVE INGREDIENT7NF3GE7IWR1
COPPERACTIVE INGREDIENT789U1901C51
DELPHINIUM STAPHISAGRIA SEEDACTIVE INGREDIENT00543AP1JV1
EPINEPHRINEACTIVE INGREDIENTYKH834O4BH1
FRAXINUS AMERICANA BARKACTIVE INGREDIENT0B24UR1O1S1
HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICEACTIVE INGREDIENTIQV54TN60Y1
LACTIC ACIDACTIVE INGREDIENT33X04XA5AT1
PETROSELINUM CRISPUMACTIVE INGREDIENT1WZA4Y92EX1
PICRIC ACIDACTIVE INGREDIENTA49OS0F91S1
POTASSIUM CARBONATEACTIVE INGREDIENTBQN1B9B9HA1
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALIX NIGRA BARKACTIVE INGREDIENTQU52J3A5B31
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
URANYL NITRATE HEXAHYDRATEACTIVE INGREDIENT3V057702FY1
ANAGALLIS ARVENSISACTIVE MOIETY46883LR90E1
ANHYDROUS CITRIC ACIDACTIVE MOIETYXF417D3PSL1
AQUA REGIAACTIVE MOIETYX3TT5X989E1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZB1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7D1
CHAMAEMELUM NOBILEACTIVE MOIETY7NF3GE7IWR1
COPPERACTIVE MOIETY789U1901C51
DELPHINIUM STAPHISAGRIA SEEDACTIVE MOIETY00543AP1JV1
EPINEPHRINEACTIVE MOIETYYKH834O4BH1
FRAXINUS AMERICANA BARKACTIVE MOIETY0B24UR1O1S1
HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICEACTIVE MOIETYIQV54TN60Y1
LACTIC ACIDACTIVE MOIETY33X04XA5AT1
PETROSELINUM CRISPUMACTIVE MOIETY1WZA4Y92EX1
PICRIC ACIDACTIVE MOIETYA49OS0F91S1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
SALIX NIGRA BARKACTIVE MOIETYQU52J3A5B31
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
URANIUM CATION (6+)ACTIVE MOIETY5PI36AS4G71
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64616-08664616-086-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62023-12-28full-release2026-06-01 02:25:16

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Category VIMMUNE SYSTEM BOOSTERVitality Works, Inc,0d3dd923-336c-4ccd-a344-ec49b2e80d102025-12-17WarningsExact identifier
ndc (package): 64616-086-02
ndc (product): 64616-086
ndc11 (package): 64616008602
spl id: 462f4405-7d7f-d581-e063-6294a90abe86
spl set id: 0d3dd923-336c-4ccd-a344-ec49b2e80d10

Reported adverse events (FAERS/openFDA)#

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