- Product NDC
- 59667-0002
- 11-digit product format
- 596670002
- Labeler code
- 59667
- Product ID
- 59667-0002_07da46df-30c7-4944-b2ca-867a60dab300
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia, Bryonia, Borax, Candida A, Calendula, Hydrastis, Kali Chloricum, Mercurius Sol, Nat Mur, Nux Moschata, Nux Vomica, Phosphorus, Saccharum Album, Sulphuricum Acidum, Staphysagria,
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Home Sweet Homeopathics
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-08-05
- Marketing end
- 0000-00-00
- Substance
- BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; SODIUM BORATE; CANDIDA ALBICANS; CALENDULA OFFICINALIS FLOWERING TOP; GOLDENSEAL; POTASSIUM CHLORATE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; NUTMEG; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SUCROSE; SULFURIC ACID; DELPHINIUM STAPHISAGRIA SEED
- Active strength
- 30 [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record