Borrelia Babesia Remedy
- Product NDC
- 43742-0246
- 11-digit product format
- 437420246
- Labeler code
- 43742
- Product ID
- 43742-0246_665b1193-796b-4b7d-93d8-06a0b8ab1a4c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Babesia Microti, Borrelia Burgdorferi Nosode
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-08-20
- Marketing end
- 2020-09-09
- Substance
- BABESIA MICROTI; BORRELIA BURGDORFERI
- Active strength
- 15 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record