Zephrex D
- Product NDC
- 0113-0401
- 11-digit product format
- 001130401
- Labeler code
- 0113
- Product ID
- 0113-0401_28086f51-f7d5-4c69-ad06-49aa164db301
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pseudoephedrine hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-11-04
- Substance
- PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zephrex D
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PSEUDOEPHEDRINE HYDROCHLORIDE | 30 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6V9V2RYJ8N | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5468a7e2-361b-494f-9ca3-1b62f3819f65 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ba088a92-ab5e-b2d4-e908-f5ea691b7587 | Product name | 7 | 20210201 |
| 0fdb98e2-b951-a1ce-5715-2b187ba500ef | Product name | 4 | 20170718 |
| e974e22d-8688-7d92-1e87-40c1079e170c | Product name | 3 | 20151125 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 30c51294-7ae9-8007-7de6-58222684a0be | Product name | 1 | 20140508 |
| 4f26f669-fc6c-40ef-9e26-1c7b2390ee66 | Product name | 1 | 20140508 |
| 70a83adc-6047-bbea-5a08-dfd304aa47d2 | Product name | 1 | 20140508 |
| 858ce051-9941-aafc-8c7c-44a8e0227463 | Product name | 1 | 20140508 |
| b893258d-0942-3d8a-3411-056ea0788ff5 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0113-0401-62 | Zephrex D | 1 in 1 BLISTER PACK | CAPSULE, GELATIN COATED | 1 | 5 | |
| 0113-0401-62 | Zephrex D | 24 in 1 CARTON | CAPSULE, GELATIN COATED | 24 | 5 | |
| 0113-0401-67 | Zephrex D | 1 in 1 BLISTER PACK | CAPSULE, GELATIN COATED | 1 | 5 | |
| 0113-0401-67 | Zephrex D | 48 in 1 CARTON | CAPSULE, GELATIN COATED | 48 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0113-0401-62 | EA - Each | 0113-0401 | 44f4e884-befd-4206-862f-cf9d09dc39a3 | 1 | 2021-04-08 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SUGAR FREE ORIGINAL SWISS HERB COUGH SUPPRESSANT THROAT DROPS | MENTHOL | Ricola Ag | b790a91c-33be-4bc3-bdeb-eae6f366f085 | 2024-12-05 | Warnings | M012 |
| EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT | MENTHOL | Ricola Ag | ea42e516-2ef8-41c9-ae4e-571f0147bc6b | 2024-12-05 | Warnings | M012 |
| RICOLA MAX THROAT CARE SWISS CHERRY | MENTHOL | Ricola Ag | 8b2d5c0f-509e-447d-b071-d73c4785f120 | 2024-12-05 | Warnings | M012 |
| SUGAR FREE GREEN TEA WITH ECHINACEA COUGH SUPPRESSANT THROAT DROPS | MENTHOL | Ricola Ag | 8ae0e21a-44a0-4a2c-9880-54eeeaea07ea | 2024-12-05 | Warnings | M012 |
| MOUNTAIN HERB SUGAR FREE WITH STEVIA COUGH SUPPRESSANT ORAL ANESTHETIC | MENTHOL | Ricola Ag | 6d82469b-d51c-4824-9830-6c1874ad4fe4 | 2024-12-05 | Warnings | M012 |
| RICOLA MAX THROAT CARE COOL PEPPERMINT | MENTHOL | Ricola Ag | e8bedf6f-4a2e-4a76-ba8c-bdb249fb6ce5 | 2024-12-05 | Warnings | M012 |
| DUAL ACTION HONEY LEMON COUGH SUPPRESSANT ORAL ANESTHETIC | MENTHOL | Ricola Ag | a535717d-ba55-45e9-9fc3-711b5d7dbf57 | 2024-12-05 | Warnings | M012 |
| THE ORIGINAL NATURAL HERB COUGH DROPS | MENTHOL | Ricola Ag | 4330ee8d-0b37-4a93-886b-5fc6e6598da7 | 2024-12-05 | Warnings | M012 |
| COLD AND FLU DAYTIME SEVERE | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | TARGET CORP | 9de99931-31ef-79e2-e053-2a95a90a98ad | 2024-12-04 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | TopCo Associates LLC | 3ef6d155-b95b-4b30-87a8-8ed811b1520f | 2024-12-03 | Warnings | M012 |
| Sinus plus Headache | ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE | TOPCARE | a1b2b16d-c767-2945-e053-2995a90a4834 | 2024-12-03 | Warnings | M012 |
| Sinus Congestion and Pain Severe | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | TopCare | fa9b2748-0474-4a39-a2b8-bb6f0678c1d1 | 2024-12-03 | Warnings | M012 |
| Sinus Pressure plus Pain PE | ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE | TOPCO ASSOCIATES LLC | a9640e09-369c-3c55-e053-2a95a90aebd5 | 2024-12-03 | Warnings | M012 |
| Cold Max | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | TOPCO ASSOCIATES LLC | ec7e5e2e-23c7-32ae-e053-2995a90a1251 | 2024-12-03 | Warnings | M012 |
| COLD AND FLU SEVERE | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | TOPCARE | cbb179c8-31fb-4a3a-9f23-4024350f8b7f | 2024-12-03 | Warnings | M012 |
| Allergy Multi Symptom | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE HYDROCHLORIDE | TOPCO ASSOCIATES LLC | a96431a0-b05d-4812-e053-2a95a90a5af6 | 2024-12-03 | Warnings | M012 |
| Cold Max Nighttime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | TopCo Associates LLC | aa0d6762-b803-4630-8f74-780b7ea9acff | 2024-12-03 | Warnings | M012 |
| Cold plus Head Congestion | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | TOPCO ASSOCIATES LLC | ec7e5e2e-23c5-32ae-e053-2995a90a1251 | 2024-12-03 | Warnings | M012 |
| Cold Plus Head Congestion Day and Night | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | TopCo Associates LLC | 898eb1c7-395a-4845-9d0a-719fc78d86b7 | 2024-12-03 | Warnings | M012 |
| Cold Plus Head Congestion Nighttime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | TopCo Associates LLC | 7854c1fd-b5fc-477d-a79e-ff006ebf6fe5 | 2024-12-03 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1430169 | pseudoephedrine HCl 30 MG Oral Capsule | PSN | 5468a7e2-361b-494f-9ca3-1b62f3819f65 | 5 |
| 1918218 | Zephrex-D 30 MG Oral Capsule | PSN | 5468a7e2-361b-494f-9ca3-1b62f3819f65 | 5 |
| 1918218 | pseudoephedrine hydrochloride 30 MG Oral Capsule [Zephrex-D] | SBD | 5468a7e2-361b-494f-9ca3-1b62f3819f65 | 5 |
| 1430169 | pseudoephedrine hydrochloride 30 MG Oral Capsule | SCD | 5468a7e2-361b-494f-9ca3-1b62f3819f65 | 5 |
| 1918218 | Zephrex-D 30 MG Oral Capsule | SY | 5468a7e2-361b-494f-9ca3-1b62f3819f65 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-0401-62 | 00113040162 | 24 BLISTER PACK in 1 CARTON (0113-0401-62) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK | 24 blister pack | 2017-04-17 | 0000-00-00 | No | No | Current |
| 0113-0401-67 | 00113040167 | 48 BLISTER PACK in 1 CARTON (0113-0401-67) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK | 48 blister pack | 2017-05-08 | 0000-00-00 | No | No | Current |