FDA.reportPublic FDA data

Asbestox

Product NDC
63083-6005
11-digit product format
630836005
Labeler code
63083
Product ID
63083-6005_cc463d20-4aef-4cd3-8849-ef48e8003ea8
Type
HUMAN OTC DRUG
Nonproprietary name
Asbestox
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
AMOSITE; BEEF LUNG; FERULA ASSA-FOETIDA RESIN; IODINE; IRON; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; PHOSPHORUS; SELENICEREUS GRANDIFLORUS STEM; SILICON DIOXIDE; SULFUR
Active strength
30; 6; 12; 12; 6; 12; 12; 6; 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
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Asbestox
Brand name suffix
6005
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMOSITE30 [hp_X]/59mL
BEEF LUNG6 [hp_X]/59mL
FERULA ASSA-FOETIDA RESIN12 [hp_X]/59mL
IODINE12 [hp_X]/59mL
IRON6 [hp_X]/59mL
MOSCHUS MOSCHIFERUS MUSK SAC RESIN12 [hp_X]/59mL
PHOSPHORUS12 [hp_X]/59mL
SELENICEREUS GRANDIFLORUS STEM6 [hp_X]/59mL
SILICON DIOXIDE12 [hp_X]/59mL
SULFUR12 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii321T905Y7I, 2I1RTO1MBR, W9FZA51AS1, 9679TC07X4, E1UOL152H7, 8KFK4W7KP7, 27YLU75U4W, 7114SV0MYK, ETJ7Z6XBU4, 70FD1KFU70

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6005-22026-01-09C16284748780-11030e365-33c4-111a-e063-dadaa90a10e2X5
63083-6005-22026-01-09C16284748780-11030e365-33c4-111a-e063-dadaa90a10e2X5
63083-6005-22024-01-30C16284748780-11030e365-33c4-111a-e063-dadaa90a10e2X5
63083-6005-22024-01-30C16284748780-11030e365-33c4-111a-e063-dadaa90a10e2X5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-6005-2Asbestox600559 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-6005ASBESTOX 6005 (ASBESTOX) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220405_90bc0d00-01e4-4134-809e-e216fd09852a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-6005-26308360050259 mL in 1 BOTTLE, DROPPER (63083-6005-2) 59 ml1985-08-150000-00-00NoNoCurrent