FDA.reportPublic FDA data

Viatrexx-F gus

Product NDC
63776-175
11-digit product format
637760175
Labeler code
63776
Product ID
63776-175_ad72d2aa-e5bf-4c61-a80d-641b2e201895
Type
HUMAN OTC DRUG
Nonproprietary name
berberis, cochlerearia armor, echinacea, ferrum, hydrastis, iridium, lapacho, lomatium, lycopodium, myrrh, phosporicum acidum, propolis, pulsatilla, seleneium, thymus, zinc
Dosage form
SPRAY
Route
ORAL; TOPICAL
Labeler
VIATREXX BIO INCORPORATED
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-03-29
Marketing end
0000-00-00
Substance
ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; SELENIUM; SUS SCROFA THYMUS; BOS TAURUS THYMUS; ZINC; BERBERIS VULGARIS ROOT BARK; ARMORACIA RUSTICANA WHOLE; IRON; IRIDIUM; HANDROANTHUS IMPETIGINOSUS WHOLE; LOMATIUM DISSECTUM ROOT; MYRRH; PHOSPHORIC ACID; PROPOLIS WAX; ANEMONE PULSATILLA
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63776-175-112022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-142022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-152022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-162022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-172022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-182022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-192022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63776-175-11Viatrexx-F gus0.5 mL in 1 AMPULESPRAY0.51
63776-175-14Viatrexx-F gus30 mL in 1 BOTTLESPRAY301
63776-175-15Viatrexx-F gus50 mL in 1 BOTTLESPRAY501
63776-175-16Viatrexx-F gus100 mL in 1 BOTTLESPRAY1001
63776-175-17Viatrexx-F gus250 mL in 1 BOTTLESPRAY2501
63776-175-18Viatrexx-F gus500 mL in 1 BOTTLESPRAY5001
63776-175-19Viatrexx-F gus1000 mL in 1 BOTTLESPRAY10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63776-175VIATREXX-F GUS (BERBERIS, COCHLEREARIA ARMOR, ECHINACEA, FERRUM, HYDRASTIS, IRIDIUM, LAPACHO, LOMATIUM, LYCOPODIUM, MYRRH, PHOSPORICUM ACIDUM, PROPOLIS, PULSATILLA, SELENEIUM, THYMUS, ZINC) SPRAY [VIATREXX BIO INCORPORATED]1Legacy NDC, 7 package rows20210227_03caaf56-536f-42a8-baed-45263431ee46.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63776-175-1163776017511.5 mL in 1 AMPULE (63776-175-11) 2021-02-240000-00-00NoNoCurrent
63776-175-146377601751430 mL in 1 BOTTLE (63776-175-14) 30 ml2021-02-240000-00-00NoNoCurrent
63776-175-156377601751550 mL in 1 BOTTLE (63776-175-15) 50 ml2021-02-240000-00-00NoNoCurrent
63776-175-1663776017516100 mL in 1 BOTTLE (63776-175-16) 100 ml2021-02-240000-00-00NoNoCurrent
63776-175-1763776017517250 mL in 1 BOTTLE (63776-175-17) 250 ml2021-02-240000-00-00NoNoCurrent
63776-175-1863776017518500 mL in 1 BOTTLE (63776-175-18) 500 ml2021-02-240000-00-00NoNoCurrent
63776-175-19637760175191000 mL in 1 BOTTLE (63776-175-19) 1000 ml2021-02-240000-00-00NoNoCurrent