BM Sepia

Product NDC
85816-5092
Requested package NDC
85816-5092-1
11-digit product format
858165092
Labeler code
85816
Product ID
85816-5092_5c56a0cb-69d5-fb96-e063-6394a90aad7e
Type
HUMAN OTC DRUG
Nonproprietary name
Sepia
Dosage form
GLOBULE
Route
ORAL
Labeler
BM Private Limited
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
SEPIA OFFICINALIS JUICE
Active strength
30 [hp_C]/1000mg
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
BM Sepia
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SEPIA OFFICINALIS JUICE30 [hp_C]/1000mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-5092-1BM Sepia30000 mg in 1 BOTTLE, GLASSGLOBULE300001

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
BM SepiaSEPIABM Private Limited38e2c6f3-1ae5-57ed-e063-6394a90a9f652025-07-01WarningsExact identifier
ndc (package): 85816-5092-1
ndc (product): 85816-5092
ndc11 (package): 85816509201

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85816-5092-18581650920130000 mg in 1 BOTTLE, GLASS (85816-5092-1) 30000 mg2015-01-01NoNoCurrent