Breatheze
- Product NDC
- 48951-2079
- 11-digit product format
- 489512079
- Labeler code
- 48951
- Product ID
- 48951-2079_6a861315-d9c9-4400-e053-2a91aa0aeef7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Breatheze
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PAPRIKA; EUPHRASIA STRICTA; LONICERA DASYSTYLA FLOWER BUD; JUJUBE FRUIT; URTICA DIOICA ROOT; URTICA DIOICA LEAF
- Active strength
- 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record