Vortex Moisturizer Nasal
- Product NDC
- 82529-000
- 11-digit product format
- 825290000
- Labeler code
- 82529
- Product ID
- 82529-000_d9a1828b-0288-0a20-e053-2a95a90a4838
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- NASAL
- Labeler
- Vortex Life Sciences, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-03-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 7 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82529-000-01 | Vortex Moisturizer Nasal | 15 mL in 1 BOTTLE | LIQUID | 15 | | 1 |
| 82529-000-01 | Vortex Moisturizer Nasal | 1 in 1 BOX | LIQUID | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82529-000 | VORTEX MOISTURIZER NASAL (SODIUM CHLORIDE) LIQUID [VORTEX LIFE SCIENCES, INC.] | 1 | Legacy NDC, 2 package rows | 20220308_d87f20d6-933f-4419-b035-e307a13a60aa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82529-000-01 | 82529000001 | 1 BOTTLE in 1 BOX (82529-000-01) > 15 mL in 1 BOTTLE | 1 bottle | 2022-03-01 | 0000-00-00 | No | No | Current |