OHTrust Artifical Eyedrop
- Product NDC
- 70970-008
- 11-digit product format
- 709700008
- Labeler code
- 70970
- Product ID
- 70970-008_2ea26d96-704c-17bb-e063-6394a90a7e27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Labeler
- Nanoplus Limited (Cayman) Taiwan Branch
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-27
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OHTrust Artifical Eyedrop
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 9 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 2706648 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70970-008-01 | OHTrust Artifical Eyedrop | 15 mL in 1 BOTTLE | LIQUID | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70970-008 | OHTRUST ARTIFICAL EYEDROP (SODIUM CHLORIDE) LIQUID [NANOPLUS LIMITED (CAYMAN) TAIWAN BRANCH] | 1 | Current NDC, 1 package rows | 20250306_2ea26d96-704b-17bb-e063-6394a90a7e27.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70970-008-01 | 70970000801 | 15 mL in 1 BOTTLE (70970-008-01) | 15 ml | 2025-02-27 | No | No | Current |