Aloe socotrina 200C

Product NDC
69152-1077
11-digit product format
691521077
Labeler code
69152
Product ID
69152-1077_39b64712-7a26-1903-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Aloe socotrina
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-03
Marketing end
0000-00-00
Substance
ALOE
Active strength
200 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1077-12020-01-31C16284748780-19d75b9d1-27f0-f424-e053-dadaa90a57ce179a83ee-ead4-5734-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1077-1Aloe socotrina 200C96 in 1 BOTTLEPELLET966

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1077ALOE SOCOTRINA 200C (ALOE SOCOTRINA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]6Legacy NDC, 1 package rows20160810_179a83ee-ead4-5734-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1077-16915210770196 in 1 BOTTLEHistorical