FDA.reportPublic FDA data

Anti-Rheumatic Formula

Product NDC
63083-2070
11-digit product format
630832070
Labeler code
63083
Product ID
63083-2070_d37bf6df-90e3-4e30-a8ac-17078b75a482
Type
HUMAN OTC DRUG
Nonproprietary name
Anti-Rheumatic Formula
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ACONITUM CARMICHAELI LATERAL ROOT; ANGELICA ACUTILOBA ROOT; CLEMATIS RECTA FLOWERING TOP; FRANKINCENSE; MYRRH; SOLANUM NIGRUM TOP; SUS SCROFA LUNG
Active strength
3; 3; 3; 3; 3; 3; 3 [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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Anti-Rheumatic Formula 2070ANTI-RHEUMATIC FORMULAProfessional Complementary Health Formulasd2d9b212-e5e5-4d4a-bec3-54875f51659d2026-01-08WarningsExact identifier
ndc (product): 63083-2070

Additional Listing Data#

Finished product
Yes
Brand name base
Anti-Rheumatic Formula
Brand name suffix
2070
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM CARMICHAELI LATERAL ROOT3 [hp_X]/59mL
FRANKINCENSE3 [hp_X]/59mL
SOLANUM NIGRUM TOP3 [hp_X]/59mL
MYRRH3 [hp_X]/59mL
ANGELICA ACUTILOBA ROOT3 [hp_X]/59mL
SUS SCROFA LUNG3 [hp_X]/59mL
CLEMATIS RECTA FLOWERING TOP3 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2A9PW94VJXInternal UNII lookup
R9XLF1R1WMInternal UNII lookup
O4G5C1G3W5Internal UNII lookup
JC71GJ1F3LInternal UNII lookup
3W51R3EK30Internal UNII lookup
7GL3G1COB3Internal UNII lookup
396421SP9FInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d2d9b212-e5e5-4d4a-bec3-54875f51659dAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2070-22026-01-09C16284748780-11030e364-ff08-111a-e063-dadaa90a10e2C70
63083-2070-22026-01-09C16284748780-11030e364-ff08-111a-e063-dadaa90a10e2C70
63083-2070-22024-01-30C16284748780-11030e364-ff08-111a-e063-dadaa90a10e2C70
63083-2070-22024-01-30C16284748780-11030e364-ff08-111a-e063-dadaa90a10e2C70

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2070-2Anti-Rheumatic Formula207059 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2070ANTI-RHEUMATIC FORMULA 2070 (ANTI-RHEUMATIC FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220216_d2d9b212-e5e5-4d4a-bec3-54875f51659d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2070-26308320700259 mL in 1 BOTTLE, DROPPER (63083-2070-2) 59 ml1985-08-150000-00-00NoNoCurrent