Control Remedy Water
- Product NDC
- 35378-0006
- 11-digit product format
- 353780006
- Labeler code
- 35378
- Product ID
- 35378-0006_a1446b4f-37d5-ce89-d211-d7a4ac858ac0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anacardium orientale, Antimon. crud., Arg. nit., Berber. vulg., Bryonia, Chelidonium majus, Digitalis, Graphites, Humulus, Iris Versicolor,
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Georgetown Health, LLC DBA EssentiaLife
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-07-01
- Marketing end
- 0000-00-00
- Substance
- SEMECARPUS ANACARDIUM JUICE; ANTIMONY TRISULFIDE; SILVER NITRATE; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; DIGITALIS; GRAPHITE; HOPS; IRIS VERSICOLOR ROOT; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; SODIUM CARBONATE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; SCUTELLARIA LATERIFLORA; SEPIA OFFICINALIS JUICE; DATURA STRAMONIUM; MATRICARIA RECUTITA; PASSIFLORA INCARNATA FLOWER; VALERIAN
- Active strength
- 15 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record