Nasal Decongestant PE
- Product NDC
- 37808-453
- 11-digit product format
- 378080453
- Labeler code
- 37808
- Product ID
- 37808-453_aaf80492-fe95-40dc-9695-fde6085385d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenylephrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H E B
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2005-01-14
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nasal Decongestant PE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENYLEPHRINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 04JA59TNSJ |
| Rxcui | 1049182 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-453-23 | Nasal Decongestant PE | 3 in 1 CARTON | TABLET, FILM COATED | 3 | | 14 |
| 37808-453-23 | Nasal Decongestant PE | 24 in 1 BLISTER PACK | TABLET, FILM COATED | 24 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PHENYLEPHRINE HYDROCHLORIDE | ACTIVE INGREDIENT | 04JA59TNSJ | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| PHENYLEPHRINE | ACTIVE MOIETY | 1WS297W6MV | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| CARBOXYMETHYLCELLULOSE SODIUM | INACTIVE INGREDIENT | K679OBS311 | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| DEXTROSE MONOHYDRATE | INACTIVE INGREDIENT | LX22YL083G | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| MALTODEXTRIN | INACTIVE INGREDIENT | 7CVR7L4A2D | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-453 | NASAL DECONGESTANT PE (PHENYLEPHRINE HCL) TABLET, FILM COATED [H E B] | 13 | Current NDC, Legacy NDC, 2 package rows | 20241206_7c04ab14-af28-4598-90ef-56ac11902c7d.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 |
|---|
| 37808-453-23 | 37808045323 | 3 BLISTER PACK in 1 CARTON (37808-453-23) / 24 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2005-01-14 | 0000-00-00 | No | No | Current |