4 Way
- Product NDC
- 0067-2086
- 11-digit product format
- 000672086
- Labeler code
- 0067
- Product ID
- 0067-2086_43684c76-26b5-24c9-e063-6294a90a9b46
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenylephrine hydrochloride
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- Haleon US Holdings LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-01-01
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- 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
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | 0067-2086 | I | Inactivated by FDA | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… | ||
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 0067-2086 | 0067-2086-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
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
- 4 Way
- Brand name suffix
- Fast Acting
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | 10 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 04JA59TNSJ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1087043 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| a8fc41c7-4425-41b8-b1c6-eb22ac054734 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e4e263da-1c53-440f-bb80-b7a575843b5a | Product name | 1 | 20260313 |
| d2168cac-a261-415a-9c78-3522859fa720 | Product name | 3 | 20251124 |
| 05a8cdd1-eeb8-409e-b938-0778225eca7d | Product name | 4 | 20250221 |
| e5b5c132-b15d-435b-9faa-2f74e5cadcf9 | Product name | 8 | 20250220 |
| f489e8f3-5c9e-4818-b539-a73587edcfc7 | Product name | 2 | 20240229 |
| 0f7ae452-206d-4fc4-868d-56fc47074084 | Product name | 1 | 20231011 |
| b5abe2e3-39a1-43eb-9bff-f3c1653fe3df | Product name | 2 | 20190930 |
| e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814 | Product name | 3 | 20150910 |
| 42f3c020-f1b3-89bc-7bdc-e1f10e680485 | Product name | 1 | 20140508 |
| e949165d-714d-e548-2b76-0cb5def16f30 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0067-2086-01 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-2e25-fb37-e063-e6dba90a4e07 | Drug Facts |
| 0067-2086-01 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-2e25-fb37-e063-e6dba90a4e07 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0067-2086-01 | 4 WayFast Acting | 29.6 mL in 1 BOTTLE, SPRAY | SPRAY | 29.6 | 13 | |
| 0067-2086-01 | 4 WayFast Acting | 1 in 1 CARTON | SPRAY | 1 | 13 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0067-2086-01 | ML - Milliliter | 0067-2086 | c086c908-628d-4743-84e6-3d43fe57b914 | 1 | 2012-07-24 |
| 0067-2086-05 | ML - Milliliter | 0067-2086 | 69981360-0504-4153-a7f4-eb82aa864002 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | ACTIVE INGREDIENT | 04JA59TNSJ | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 | |
| PHENYLEPHRINE | ACTIVE MOIETY | 1WS297W6MV | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 | |
| BENZALKONIUM CHLORIDE | INACTIVE INGREDIENT | F5UM2KM3W7 | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 | |
| BORIC ACID | INACTIVE INGREDIENT | R57ZHV85D4 | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 | |
| SODIUM BORATE | INACTIVE INGREDIENT | 91MBZ8H3QO | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 4 WAY FAST ACTING (PHENYLEPHRINE HYDROCHLORIDE) SPRAY [NOVARTIS CONSUMER HEALTH, INC.] | 2 |
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 |
|---|---|---|---|---|---|---|
| CareAll Medicated Chest Rub | CAMPHOR, MENTHOL, EUCALYPTUS | New World Imports, Inc | 4cd2f751-e072-4f4e-b059-ed1dfcc60c6b | 2025-12-01 | Warnings | M012 |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | CVS PHARMACY, INC | bbb1b395-48d9-4859-ad52-6650961089d9 | 2025-12-01 | Warnings | M012 |
| Severe Sinus Pain and Congestion | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | fbc541ac-9465-4296-bb1e-811b9d811f40 | 2025-11-26 | Warnings | M012 |
| Daytime Severe and Nighttime Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Grocery Outlet, Inc. | 447951e6-459d-0a52-e063-6294a90a6226 | 2025-11-26 | Warnings | M012 |
| Daytime Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBR, GUAIFENESIN PHENYLEPHRINE HCL | WALGREENS CO. | bfc58cd5-9815-43af-895d-ec6cbd10937e | 2025-11-26 | Warnings | M012 |
| Walgreen Cough and Chest Congestion | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | WALGREEN COMPANY | 40c038a3-91c7-4ed0-8210-65d58b82ca2b | 2025-11-26 | Warnings | M012 |
| Mucus Relief DM Maximum Strength | DEXTROMETHORPHAN HBR AND GUAIFENESIN | WALGREENS CO | 724554ab-60b8-46c8-96a8-a98242604e3b | 2025-11-26 | Warnings | M012 |
| Walgreens Grape Flavor | CHILDREN COUGH AND CHEST CONGESTION | WALGREENS | 795cf1af-3847-46bc-b605-64a38e57cca2 | 2025-11-26 | Warnings | M012 |
| Walgreens | CHILDRENS STUFFY NOSE AND COLD | WALGREENS CO. | 7ac3de2d-1d10-49ec-a2da-da46977684ad | 2025-11-26 | Warnings | M012 |
| Childrens Chest Congestion Relief | GUAIFENESIN | WALGREENS COMPANY | c1382512-e6f3-4bdf-a9e6-4f68dd5ea553 | 2025-11-26 | Warnings | M012 |
| Dye Free Wal Sleep Z | DIPHENHYDRAMINE HYDROCHLORIDE | WALGREEN CO. | 96948973-09e3-4c05-8982-0494ebeaac4b | 2025-11-26 | Warnings | M012 |
| WALGREEN ADULT COUGH PLUS CHEST CONGESTION DM | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | WALGREEN COMPANY | 02ad9f98-07ad-4786-a1ab-169b870fec01 | 2025-11-26 | Warnings | M012 |
| Walgreen Cherry | GUAIFENESIN | WALGREEN COMPANY | 1f1cb4a5-1ebd-483c-bf82-16931da00e05 | 2025-11-26 | Warnings | M012 |
| Walgreen Childrens COLD PLUS COUGH PLUS SORE THROAT | ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE | WALGREENS CO. | 801880b2-6116-4d26-a7bf-a669eef6ad8b | 2025-11-26 | Warnings | M012 |
| Walgreen Daytimel Kids Cold Cough plus Mucus | GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE | WALGREENS CO. | 452159e0-1204-460c-981f-cace4e815c6f | 2025-11-26 | Warnings | M012 |
| Multi Symptom Wal Flu Severe Cold | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | WALGREEN CO. | 9c0f3f1e-25d1-4d73-9cd7-42708aa66dcb | 2025-11-25 | Warnings | M012 |
| WALGREEN Daytime Multi Symptom Flu Relief Max Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | WALGREENS CO. | c92a0f47-0b7c-4034-83d1-b7d2ed8022fc | 2025-11-25 | Warnings | M012 |
| Mucus Relief DM Honey and Berry Flavor | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | WALGREENS CO. | 428081f5-b7eb-42da-963c-a587a44b2a79 | 2025-11-25 | Warnings | M012 |
| Walgreen NightTime Cold and Flu relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDE | WALGREENS CO. | 6b3766e6-d0d4-49e0-90da-fc893aef3329 | 2025-11-25 | Warnings | M012 |
| Adult Allergy Relief Dye Free | DIPHENHYDRAMINE HYDROCHLORIDE | WALGREEN COMPANY | 586310f3-0014-4cfc-9d86-961b3fb7aa8c | 2025-11-25 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1087043 | phenylephrine HCl 1 % Nasal Spray | PSN | a8fc41c7-4425-41b8-b1c6-eb22ac054734 | 13 |
| 1087043 | phenylephrine hydrochloride 10 MG/ML Nasal Spray | SCD | a8fc41c7-4425-41b8-b1c6-eb22ac054734 | 13 |
| 1087043 | phenylephrine hydrochloride 1 % Nasal Spray | SY | a8fc41c7-4425-41b8-b1c6-eb22ac054734 | 13 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0067-2086-01 | 00067208601 | 1 BOTTLE, SPRAY in 1 CARTON (0067-2086-01) / 29.6 mL in 1 BOTTLE, SPRAY | 2010-01-01 | 0000-00-00 | No | No | Current |