Supress DM
- Product NDC
- 52083-058
- 11-digit product format
- 520830058
- Labeler code
- 52083
- Product ID
- 52083-058_974dbf24-7689-4e94-a535-d5b59c097406
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- dextromethorphan hydrobromide, guaifenesin
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- KRAMER NOVIS
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-10-02
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 50; 5 mg/mL; mg/mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- 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 | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 52083-058-01 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 52083-058-01 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 52083-058-01 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 52083-058-01 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 52083-058-01 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 52083-058-01 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 52083-058-01 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 52083-058-01 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
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
- Supress DM
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 50 mg/mL |
| DEXTROMETHORPHAN HYDROBROMIDE | 5 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 495W7451VQ | Internal UNII lookup |
| 9D2RTI9KYH | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1439992 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7da0611e-729c-4cf8-88f3-f8877b9f5cfa | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bf324df6-7127-7deb-def5-2681c136cd03 | Product name | 3 | 20250325 |
| 43a1ed49-eae2-4840-8075-cb4b33478540 | Product name | 1 | 20230425 |
| ba088a92-ab5e-b2d4-e908-f5ea691b7587 | Product name | 7 | 20210201 |
| 4fe95224-f543-4dbb-9445-8cca122b48c8 | Product name | 1 | 20150609 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 106ff02a-57e1-4c4c-a307-fd582ff4e311 | Product name | 1 | 20150212 |
| 76633df9-0d59-4b88-03ed-21dee1b966f8 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52083-058-01 | 2025-11-18 | C162847 | 48780-1 | 2cef2736-5f9c-d83d-e063-dadaa90ab31f | Supress DM |
| 52083-058-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-5f9c-d83d-e063-dadaa90ab31f | Supress DM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52083-058-01 | Supress DM | 30 mL in 1 BOTTLE | SYRUP | 30 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52083-058-01 | ML - Milliliter | 52083-058 | 9db1418f-5f10-40ad-9fa8-1f0b9c5e8a85 | 1 | 2013-12-02 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|
| 1439992 | dextromethorphan HBr 5 MG / guaiFENesin 50 MG in 1 mL Oral Solution | PSN | 7da0611e-729c-4cf8-88f3-f8877b9f5cfa | 5 |
| 1439992 | dextromethorphan hydrobromide 5 MG/ML / guaifenesin 50 MG/ML Oral Solution | SCD | 7da0611e-729c-4cf8-88f3-f8877b9f5cfa | 5 |
| 1439992 | dextromethorphan hydrobromide 5 MG/ML / GG 50 MG/ML Oral Solution | SY | 7da0611e-729c-4cf8-88f3-f8877b9f5cfa | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 52083-058-01 | 52083005801 | 30 mL in 1 BOTTLE (52083-058-01) | 30 ml | 2013-10-02 | 0000-00-00 | No | No | Current |