Non-Drowsy Nasal Decongestant PE
- Product NDC
- 70692-100
- 11-digit product format
- 706920100
- Labeler code
- 70692
- Product ID
- 70692-100_b1935570-d420-ab2e-e053-2995a90ae8d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenylephrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strive Pharmaceuticals Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-02-22
- Marketing end
- 0000-00-00
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70692-100-24 | Non-Drowsy Nasal Decongestant PE | 24 in 1 BLISTER PACK | TABLET, FILM COATED | 24 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70692-100 | NON-DROWSY NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [STRIVE PHARMACEUTICALS INC.] | 3 | Legacy NDC, 1 package rows | 20201014_64e2a606-3d47-f255-e053-2991aa0a519d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70692-100-24 | 70692010024 | 24 TABLET, FILM COATED in 1 BLISTER PACK (70692-100-24) | 2018-02-22 | 0000-00-00 | No | No | Current |