AM-3
- Product NDC
- 58264-0342
- 11-digit product format
- 582640342
- Labeler code
- 58264
- Product ID
- 58264-0342_2b530322-3436-c1f4-e063-6294a90abea4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cinchona officinalis Bark, Potassium Chlorate, and Lachesis Muta Whole
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- CINCHONA OFFICINALIS BARK; LACHESIS MUTA WHOLE; POTASSIUM CHLORATE
- Active strength
- 10; 12; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| S003A158SB | CINCHONA OFFICINALIS BARK | | CINCHONA OFFICINALIS BARK |
| 6Y582I290C | LACHESIS MUTA WHOLE | | LACHESIS MUTA WHOLE |
| H35KS68EE7 | POTASSIUM CHLORATE | 3811-04-9 | POTASSIUM CHLORATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58264-0342-1 | 58264034201 | 29.57 mL in 1 BOTTLE, GLASS (58264-0342-1) | 29.57 ml | 1990-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| AM-3 | DNA Labs, Inc. | 2025-01-09 | HUMAN OTC DRUG LABEL | 3 |