Household Antigens
- Product NDC
- 44911-0017
- 11-digit product format
- 449110017
- Labeler code
- 44911
- Product ID
- 44911-0017_bc799447-8a97-4831-ba60-2131a1c616c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetone, Sodium tripolyphosphate, Propylene glycol, Sodium benzene sulfonate, Sodium lauryl sulfate, Terebinthina,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-08-07
- Marketing end
- 2021-08-10
- Substance
- ACETONE; SODIUM TRIPOLYPHOSPHATE; PROPYLENE GLYCOL; SODIUM BENZENESULFONATE; AMMONIUM CHLORIDE; SODIUM LAURYL SULFATE; TURPENTINE OIL; BUTYL ACETATE; TOLUENE; XYLENE (MIXED ISOMERS); DIBUTYL PHTHALATE; KEROSENE; SEMECARPUS ANACARDIUM JUICE; GRAPHITE; NITRIC ACID; PULSATILLA VULGARIS WHOLE; SULFUR; ETHYL ACETATE
- Active strength
- 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0017-1 | 44911001701 | 30 mL in 1 BOTTLE, DROPPER (44911-0017-1) | 30 ml | 2012-08-07 | 2021-08-10 | No | No | Current |