Respitrol
- Product NDC
- 49726-040
- 11-digit product format
- 497260040
- Labeler code
- 49726
- Product ID
- 49726-040_ed982acf-e558-dfe4-e053-2995a90ae717
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ammonium Carbonicum, Antimonium Tartaricum, Bromium, Carbo Vegetabilis, Chlorinum, Kali Carbonicum, Lobelia Inflata, Stannum Metallicum, Sulphuricum Acidum
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HelloLife, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-06-15
- Marketing end
- 0000-00-00
- Substance
- ACTIVATED CHARCOAL; AMMONIUM CARBONATE; ANTIMONY POTASSIUM TARTRATE; BROMINE; CHLORINE; LOBELIA INFLATA; POTASSIUM CARBONATE; SULFURIC ACID; TIN
- Active strength
- 10 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49726-040-60 | 49726004060 | 60 TABLET in 1 BOTTLE, PLASTIC (49726-040-60) | 60 tablet | 2018-06-15 | 0000-00-00 | No | No | Current |