Indigo

Product NDC
37662-3695
11-digit product format
376623695
Labeler code
37662
Product ID
37662-3695_021103af-6167-d747-e063-6394a90a9b4e
Type
HUMAN OTC DRUG
Nonproprietary name
Indigo
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-03
Substance
INDIGO
Active strength
1 [hp_Q]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IndigoINDIGOHahnemann Laboratories, INC.021103af-6166-d747-e063-6394a90a9b4e2023-08-03Exact identifier

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INDIGO1 [hp_Q]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1G5BK41P4F

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3695-1Indigo10000 in 1 BOTTLE, PLASTICPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3695INDIGO PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 1 package rows20230804_021103af-6166-d747-e063-6394a90a9b4e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3695-13766236950110000 PELLET in 1 BOTTLE, PLASTIC (37662-3695-1) 10000 pellet2023-08-03NoNoCurrent