FDA.reportPublic FDA data

Metal

Product NDC
61626-0103
11-digit product format
616260103
Labeler code
61626
Product ID
61626-0103_b9491337-22f1-60be-e053-2995a90a2ca0
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminia, Ammon carb, Anacardium, Antimon crud, Hydrastis, Ignatia, Mag phos, Nat mur, Nitricum ac, Osmium, Paraffinum, Senna, Silicea, Spongia
Dosage form
LIQUID
Route
ORAL
Labeler
NET Remedies
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-12-04
Substance
ALUMINUM OXIDE; AMMONIUM CARBONATE; ANACARDIUM OCCIDENTALE FRUIT; ANTIMONY TRISULFIDE; GOLDENSEAL; MAGNESIUM PHOSPHATE, DIBASIC; NITRIC ACID; OSMIUM; PARAFFIN; SENNA LEAF; SILICON DIOXIDE; SODIUM CHLORIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; STRYCHNOS IGNATII SEED
Active strength
12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 [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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Metal
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALUMINUM OXIDE12 [hp_X]/59mL
AMMONIUM CARBONATE12 [hp_X]/59mL
ANACARDIUM OCCIDENTALE FRUIT12 [hp_X]/59mL
ANTIMONY TRISULFIDE12 [hp_X]/59mL
GOLDENSEAL12 [hp_X]/59mL
STRYCHNOS IGNATII SEED12 [hp_X]/59mL
MAGNESIUM PHOSPHATE, DIBASIC12 [hp_X]/59mL
SODIUM CHLORIDE12 [hp_X]/59mL
NITRIC ACID12 [hp_X]/59mL
OSMIUM12 [hp_X]/59mL
PARAFFIN12 [hp_X]/59mL
SENNA LEAF12 [hp_X]/59mL
SILICON DIOXIDE12 [hp_X]/59mL
SPONGIA OFFICINALIS SKELETON, ROASTED12 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 14 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
LMI26O6933Internal UNII lookup
NJ5VT0FKLJInternal UNII lookup
4A10JR4E7EInternal UNII lookup
F79059A38UInternal UNII lookup
ZW3Z11D0JVInternal UNII lookup
1NM3M2487KInternal UNII lookup
A1Y870209ZInternal UNII lookup
451W47IQ8XInternal UNII lookup
411VRN1TV4Internal UNII lookup
2E7M255OPYInternal UNII lookup
I9O0E3H2ZEInternal UNII lookup
AK7JF626KXInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
1PIP394IIDInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f7682a4e-c767-4429-98aa-e8c5ef6560a6Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
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
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61626-0103-4Metal59 mL in 1 BOTTLELIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61626-0103METAL (ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA) LIQUID [NET REMEDIES]2Current NDC, Legacy NDC, 1 package rows20210121_f7682a4e-c767-4429-98aa-e8c5ef6560a6.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
MetalALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIANET Remediesf7682a4e-c767-4429-98aa-e8c5ef6560a62021-01-19WarningsExact identifier
ndc (product): 61626-0103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61626-0103-46162601030459 mL in 1 BOTTLE (61626-0103-4) 59 ml2018-12-040000-00-00NoNoCurrent