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 |
|---|---|---|---|---|---|---|
| childrens Allergy Dye Free Wal Dryl | DIPHENHYDRAMINE HYDROCHLORIDE | WALGREEN CO. | 4e64e040-1662-4dc9-b33f-3e119e0b3f7b | 2025-11-25 | Warnings | M012 |
| Walgreen | NASAL | WALGREENS CO | d38f8406-d7b9-472c-a472-58968bbdb993 | 2025-11-25 | Warnings | M012 |
| Theraflu Flu Relief Max Strength Nighttime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Haleon US Holdings LLC | 780907b8-34ba-4ec8-bcdf-b2a31bd111df | 2025-11-25 | Warnings | M012 |
| Robitussin Elderberry Maximum Strength Cough plus Chest Congestion DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Haleon US Holdings LLC | d13efbcd-1277-45d0-8389-1ba0337f7a24 | 2025-11-25 | Warnings | M012 |
| Childrens Robitussin Elderberry Cough and Chest Congestion DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Haleon US Holdings LLC | fe903448-b422-42e0-b05b-aeb3e5481e3c | 2025-11-25 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | DOLGENCORP INC | 1d4fcb76-22d1-7292-e063-6394a90af920 | 2025-11-25 | Warnings | M012 |
| ROBITUSSIN LONG-ACTING COUGH Soft CHEWS | DEXTROMETHORPHAN HYDROBROMIDE | Haleon US Holdings LLC | f22248b7-7abd-4df7-a986-dae357ebe8f1 | 2025-11-25 | Warnings | M012 |
| ROBITUSSIN Nighttime Cough DM Soft CHEWS | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | Haleon US Holdings LLC | 39468746-e06d-4849-9d06-9af4d14351b0 | 2025-11-25 | Warnings | M012 |
| Daytime and Nighttime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | Grocery Outlet, Inc. | 4478fd51-bae3-6108-e063-6394a90a07ca | 2025-11-25 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | CHAIN DRUG MARKETING ASSOCIATION INC. | 395bb39a-e26f-f4f2-e063-6394a90ae721 | 2025-11-25 | Warnings | M012 |
| day time | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | H E B | eaf3af6a-de5b-43fe-83ff-9641646e0f6b | 2025-11-25 | Warnings | M012 |
| MUCINEX Rapid Clear Pain, Headache and Mucus Congestion and Nighttime Liquid Gels | ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | RB Health (US) LLC | 38571853-992f-9998-e063-6394a90a8581 | 2025-11-24 | Warnings | M012 |
| Basic Care Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Amazon.com Services LLC | e19b561c-fb76-4355-a306-d3dc46930bf2 | 2025-11-24 | Warnings | M012 |
| Sinus Decongestion | PSEUDOEPHEDRINE HCL | Kroger Company | 73c3a9ac-43d6-4ecd-9add-36ca1c40ba9c | 2025-11-24 | Warnings | M012 |
| Tussin Multi Symptom Cold CF | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI | Cardinal Health (Leader) 70000 | 14c507df-fbac-4a09-a66c-b91c2abbf550 | 2025-11-24 | Warnings | M012 |
| Severe Nighttime Cold and Flu Relief | ACETAMINOPHEN DEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATE PHENYLEPHRINE HCI | Family Dollar (FAMILY WELLNESS) | e5c90d6e-70aa-4886-bc81-293e0dcf5638 | 2025-11-24 | Warnings | M012 |
| Throat Coat Eucalyptus Mint | MENTHOL | Traditional Medicinals, Inc. | a7a86f1b-30e8-6f5d-e053-2a95a90a2a82 | 2025-11-21 | Warnings | M012 |
| Throat Coat Sweet Orange Fennel | MENTHOL | Traditional Medicinals, Inc. | 4538248f-11cc-d6b2-e063-6294a90a652c | 2025-11-21 | Warnings | M012 |
| up and up Daytime Nighttime Childrens Multi Symptom Cold | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DIPHENHYDRAMINE HYDROCHLORIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Target Corporation | b8a4da0b-e4d3-48e6-b699-cb56c7b67ed7 | 2025-11-20 | Warnings | M012 |
| Supress DX Pediatric Drops | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | KRAMER NOVIS | ddb95436-7806-4086-af4d-18a6625b5c83 | 2025-11-20 | 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 |