FDA.reportPublic FDA data

Sycosis Miasm Drops

Product NDC
63083-2062
11-digit product format
630832062
Labeler code
63083
Product ID
63083-2062_23e3ba23-c817-4e1e-9fbd-0a9a74efd542
Type
HUMAN OTC DRUG
Nonproprietary name
Sycosis Miasm Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ARSENIC TRIOXIDE; GONORRHEAL URETHRAL SECRETION HUMAN; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; PULSATILLA MONTANA WHOLE; SILVER NITRATE; SMILAX ORNATA ROOT; SODIUM SULFATE; THUJA OCCIDENTALIS LEAF
Active strength
30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sycosis Miasm Drops
Brand name suffix
2062
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARSENIC TRIOXIDE30 [hp_X]/59mL
GONORRHEAL URETHRAL SECRETION HUMAN30 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE30 [hp_X]/59mL
NITRIC ACID30 [hp_X]/59mL
PULSATILLA MONTANA WHOLE30 [hp_X]/59mL
SILVER NITRATE30 [hp_X]/59mL
SMILAX ORNATA ROOT30 [hp_X]/59mL
SODIUM SULFATE30 [hp_X]/59mL
THUJA OCCIDENTALIS LEAF30 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiS7V92P67HO, 9BZG9E3I8F, C88X29Y479, 411VRN1TV4, 24K790T39B, 95IT3W8JZE, 2H1576D5WG, 0YPR65R21J, 0T0DQN8786

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2062-22026-01-08C16284748780-11030e365-672d-111a-e063-dadaa90a10e2C62
63083-2062-22026-01-08C16284748780-11030e365-672d-111a-e063-dadaa90a10e2C62
63083-2062-22024-01-30C16284748780-11030e365-672d-111a-e063-dadaa90a10e2C62
63083-2062-22024-01-30C16284748780-11030e365-672d-111a-e063-dadaa90a10e2C62

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2062-2Sycosis Miasm Drops206259 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2062SYCOSIS MIASM DROPS 2062 (SYCOSIS MIASM DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220216_71b58940-fb68-49dd-a326-5d4d04279092.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2062-26308320620259 mL in 1 BOTTLE, DROPPER (63083-2062-2) 59 ml1985-08-150000-00-00NoNoCurrent