Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent
- Product NDC
- 59390-184
- 11-digit product format
- 593900184
- Labeler code
- 59390
- Product ID
- 59390-184_fc39d7b1-cea0-4702-89bd-bf63adbeb675
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Altaire Pharmaceuticals Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-03-30
- Substance
- SODIUM CHLORIDE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1298435 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59390-184-50 | Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent | 1 in 1 BOX | OINTMENT | 1 | | 1 |
| 59390-184-50 | Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent | 3.5 g in 1 TUBE | OINTMENT | 3.5 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59390-184-50 | 59390018450 | 1 TUBE in 1 BOX (59390-184-50) / 3.5 g in 1 TUBE | 1 tube | 2004-03-30 | No | No | Current |