Supress DX Pediatric Drops
- Product NDC
- 52083-055
- 11-digit product format
- 520830055
- Labeler code
- 52083
- Product ID
- 52083-055_dc1e71f8-2a20-4968-b4ad-00c19b3d0dec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- KRAMER NOVIS
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-03-29
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 5; 50; 2.5 mg/mL; mg/mL; mg/mL
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], 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], alpha-1 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
- Supress DX Pediatric Drops
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 5 mg/mL |
| GUAIFENESIN | 50 mg/mL |
| PHENYLEPHRINE HYDROCHLORIDE | 2.5 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9D2RTI9KYH | Internal UNII lookup |
| 495W7451VQ | Internal UNII lookup |
| 04JA59TNSJ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1095503 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ddb95436-7806-4086-af4d-18a6625b5c83 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52083-055-01 | Supress DX Pediatric Drops | 30 mL in 1 BOTTLE | SYRUP | 30 | 8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52083-055-01 | ML - Milliliter | 52083-055 | 3c236263-f16b-4deb-a0d6-5fbf7cf0a25e | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52083-055 | SUPRESS DX PEDIATRIC DROPS (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE) SYRUP [KRAMER NOVIS] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241011_ddb95436-7806-4086-af4d-18a6625b5c83.zip |
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 |
|---|---|---|---|---|---|---|
| Allergy Relief | DIPHENHYDRAMINE HCL | DOLGENCORP, LLC | bab078bb-f6b0-4394-84de-92b2c582b5da | 2026-01-12 | Warnings | M012 |
| Nasal Decongestant PE Non-Drowsy Maximum Strength | PHENYLEPHRINE HCL | CHAIN DRUG MARKETING ASSOCIATION INC | bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d | 2026-01-12 | Warnings | M012 |
| CVS Health Medicated Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | CVS Pharmacy | 022c3083-c611-47d0-aa93-d6c7612e7a47 | 2026-01-11 | Warnings | M012 |
| CVS Health Medicated Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | CVS Pharmacy | bf73d15a-9d68-42fa-bfee-d25748215f97 | 2026-01-11 | Warnings | M012 |
| GUAIFENESIN 400MG CAPLETS | GUAIFENESIN | Gendose Pharmaceuticals, LLC | e7b82ec7-ef23-50c1-e053-2a95a90a662f | 2026-01-10 | Warnings | M012 |
| Daytime Cold and Flu | DAYTIME COLD AND FLU | Allegiant Health | 69ed2da0-16b2-49eb-91b4-cc5cf328c817 | 2026-01-09 | Warnings | M012 |
| HyVee Cough Drops Original Herb | MENTHOL | HY-VEE, INC | 47f81e54-0ce4-439d-e063-6294a90a2abe | 2026-01-09 | Warnings | M012 |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | A-S Medication Solutions | a5809774-ed52-4f54-b48e-888631e0223d | 2026-01-09 | Warnings | M012 |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | A-S Medication Solutions | 5767f546-a751-4583-a8b7-971175c27ef0 | 2026-01-09 | Warnings | M012 |
| Thompson Cough and Cold Multi-Symptom Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE, GUAIFENESIN, , | Thompson | e77725b1-15da-35bd-e053-2a95a90ad6ba | 2026-01-08 | Warnings | M012 |
| Mucosan Childrens Multi-Symptom Grape | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 266c8cce-cdf9-557d-e063-6394a90a9bc3 | 2026-01-08 | Warnings | M012 |
| Mucosan Multi-Symptom Honey | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Menper Distributors, Inc. | 2669c620-ab70-abaa-e063-6394a90a58e7 | 2026-01-08 | Warnings | M012 |
| Mucosan Multi-Symptom Cherry | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 26b8c06d-4a72-3979-e063-6394a90a96d7 | 2026-01-08 | Warnings | M012 |
| Mucosan Max with Acetaminophen | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 26a4861b-5d8e-9ec6-e063-6394a90af577 | 2026-01-08 | Warnings | M012 |
| Mucosan Severe Multi-Symptom | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Menper Distributors, Inc. | 26a69342-f65f-cb46-e063-6394a90ade10 | 2026-01-08 | Warnings | M012 |
| HyVee Cough Drops Original Herb | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | e4e15c13-f583-4484-a5f0-f04c39c7b7c9 | 2026-01-08 | Warnings | M012 |
| Alka-Seltzer Plus Severe Cold PowerFast Fizz Non Drowsy | ASPRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE | Bayer HealthCare LLC. | a355d987-77ce-9e32-e053-2995a90a6431 | 2026-01-08 | Warnings | M012 |
| Alka-Seltzer Plus Maximum Strength Sinus, Congestion and Pain Power Max Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE , PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | e07931fc-f753-1aeb-e053-2a95a90ada3f | 2026-01-08 | Warnings | M012 |
| Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night | ASPIRIN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE | Bayer HealthCare LLC. | fc60af2f-83cb-99ea-e053-6394a90a0b3b | 2026-01-08 | Warnings | M012 |
| Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE , DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | e17eb929-209d-a2d1-e053-2a95a90a4cf3 | 2026-01-08 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1095503 | dextromethorphan HBr 5 MG / guaiFENesin 50 MG / phenylephrine HCl 2.5 MG in 1 mL Oral Solution | PSN | ddb95436-7806-4086-af4d-18a6625b5c83 | 8 |
| 1095503 | dextromethorphan hydrobromide 5 MG/ML / guaifenesin 50 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Oral Solution | SCD | ddb95436-7806-4086-af4d-18a6625b5c83 | 8 |
| 1095503 | dextromethorphan HBr 5 MG / guaifenesin 50 MG / phenylephrine HCl 2.5 MG per 1 ML Oral Drops | SY | ddb95436-7806-4086-af4d-18a6625b5c83 | 8 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 52083-055-01 | 52083005501 | 30 mL in 1 BOTTLE (52083-055-01) | 30 ml | 2011-03-29 | 0000-00-00 | No | No | Current |