Indole
- Product NDC
- 43742-0212
- 11-digit product format
- 437420212
- Labeler code
- 43742
- Product ID
- 43742-0212_81a42657-5fbd-4ba1-b29b-8035c1dda385
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Indolum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-04-03
- Marketing end
- 2020-08-24
- Substance
- INDOLE
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record