SYMBIO MUC/ASPERGILLUS DROPS

Product NDC
69710-145
11-digit product format
697100145
Labeler code
69710
Product ID
69710-145_40e5d064-ae17-7416-e063-6294a90ae6fe
Type
HUMAN OTC DRUG
Nonproprietary name
Mucor racemosus, Aspergillus niger
Dosage form
LIQUID
Route
ORAL
Labeler
Symbiopathic
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-10-08
Substance
ASPERGILLUS NIGER VAR. NIGER; MUCOR RACEMOSUS
Active strength
4; 4 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage69710-145-11ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage69710-145-11367a005e9d99…383a685ebd0f…

Additional Listing Data#

Finished product
Yes
Brand name base
SYMBIO MUC/ASPERGILLUS DROPS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MUCOR RACEMOSUS4 [hp_X]/mL
ASPERGILLUS NIGER VAR. NIGER4 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
17RH99LQ7GInternal UNII lookup
9IOA40ANG6Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0787f5d5-42ad-575b-e063-6394a90ad4ceAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-12-11MUC ASPER 4X
2024-12-11MUC ASPER 4X
2024-07-30MUC ASPER 4X
2024-07-30MUC ASPER 4X
2024-01-30MUC ASPER 4X
2024-01-30MUC ASPER 4X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69710-145-11SYMBIO MUC/ASPERGILLUS DROPS10 mL in 1 BOTTLELIQUID103
69710-145-11SYMBIO MUC/ASPERGILLUS DROPS1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69710-145SYMBIO MUC/ASPERGILLUS DROPS (MUCOR RACEMOSUS, ASPERGILLUS NIGER) LIQUID [SYMBIOPATHIC]2Current NDC, 2 package rows20241213_0787f5d5-42ad-575b-e063-6394a90ad4ce.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
SYMBIO MUC/ASPERGILLUS DROPSMUCOR RACEMOSUS, ASPERGILLUS NIGERSymbiopathic0787f5d5-42ad-575b-e063-6394a90ad4ce2025-10-11WarningsExact identifier
ndc (product): 69710-145

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69710-145-11697100145111 BOTTLE in 1 CARTON (69710-145-11) / 10 mL in 1 BOTTLE1 bottle2023-10-08NoNoCurrent