Sulphur Remedy
- Product NDC
- 43742-0179
- 11-digit product format
- 437420179
- Labeler code
- 43742
- Product ID
- 43742-0179_61bfd841-02a7-41d5-b58b-983eadf16ecf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulphur, Asclepias tuberosa, Bryonia, Dulcamara,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-12
- Marketing end
- 2020-09-15
- Substance
- SULFUR; ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM
- Active strength
- 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record