DAYTIME COLD AND FLU acetaminophen, dextromethorphan HBr, Phenylephrine HCl 325 mg/15mL; 10 mg/15mL; 5 mg/15mL Liquid, 355 mL — NDC 37835-527-12 (Billing 37835-0527-12)
This is a package of 355 mL of DAYTIME COLD AND FLU acetaminophen, dextromethorphan HBr, Phenylephrine HCl 325 mg/15mL; 10 mg/15mL; 5 mg/15mL Liquid from BI-MART, marketed since May 2025 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 37835-527-12 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 37835 labeler · 527 product · 12 package
- Package marketed since
- May 1, 2025
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC)
- 0071357912445
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1113705
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Anilides class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Acetaminophen is used to relieve mild to moderate pain and to reduce fever. Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
Read the full MedlinePlus article ↗This is an oral liquid cold and flu product that combines three active ingredients. Acetaminophen is typically used to reduce fever and relieve pain, while dextromethorphan is commonly used as a cough suppressant. Phenylephrine functions as a decongestant, meant to help relieve nasal congestion. This product is an over-the-counter monograph drug, which means it is marketed under FDA's established rules for this category of medicine.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 5, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 37835-0527-12 You're viewing this Main listing | 355 mL in 1 BOTTLE | 2025-05-01 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
What it looks like
Where does this data come from?
- FDA label on DailyMed · label index refreshed Oct 5, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 2968PHW8QP
A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
-
UNII H77VEI93A8
A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
-
UNII PDC6A3C0OX
Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
-
UNII L7T10EIP3A
A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
-
UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII OJ245FE5EU
Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
-
UNII 8KW3E207O2
A liquid sweetener made from sorbitol, a sugar alcohol derived from glucose. It sweetens the medicine and also acts as a humectant to help retain moisture and improve texture in liquid formulations.
-
UNII 96K6UQ3ZD4
Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
-
UNII TTV12P4NEE
Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
10 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 5, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from BI-MART labeler code 37835
- Diphenhydramine HCl 50 mg/30mL Liquid NDC 37835-519-12
- Daytime Cold and Flu Relief acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride 325 mg; 10 mg; 5 mg Capsule, Liquid Filled NDC 37835-520-24
- Nighttime Cold and Flu Relief Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr 325 mg; 15 mg; 6.25 mg Capsule, Liquid Filled NDC 37835-522-24
- Cold and Flu Nighttime Acetaminophen, Dextromethorphan HBr, Doxylamine succinate 650 mg/30mL; 30 mg/30mL; 12.5 mg/30mL Solution NDC 37835-524-02
- NIGHTTIME COLD AND FLU Acetaminophen, Doxylamine succinate and Dextromethorphan HBr 650 mg/30mL; 30 mg/30mL; 12.5 mg/30mL Liquid NDC 37835-525-12
- Cold and Flu Daytime Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl 325 mg/15mL; 10 mg/15mL; 5 mg/15mL Solution NDC 37835-526-02
- Acetaminophen, Aspirin, and Caffeine 250 mg; 250 mg; 65 mg Tablet NDC 37835-531-01
- Acetaminophen and Diphenhydramine Hydrochloride 500 mg; 25 mg Tablet NDC 37835-537-01
- Adult Low Dose Enteric Coated Aspirin 81 mg Tablet, Delayed Release NDC 37835-571-05
- Low Dose Chewable Aspirin 81 mg Tablet, Chewable NDC 37835-573-36
- Aspirin 325 mg Tablet, Film Coated NDC 37835-577-01
- Ibuprofen 200 mg Tablet NDC 37835-581-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses temporarily relieves common cold and flu symptoms: minor aches and pains headache sore throat fever nasal congestion cough due to minor throat and bronchial irritation
⏱️ Dosage and Administration ▾
Directions take only as directed (see Overdose warning) measure only with dose cup provided and keep dose cup with product mL=mililiter do not exceed 4 doses per 24 hours Age Dose adults & children 12 years and over 30 mL every 4 hours children 6 to under 12 years 15 mL every 4 hours children under 6 years do not use
⚠️ Warnings ▾
Warnings Liver warning: This product contains acetaminophen. Sever liver damage may occur if: adults and children over 12 years of age take more than 4 doses (30 mL each) in 24 hours, which is the maximum daily amount for this product children 6 to 12 years of age take more than 4 doses (15 mL each) in 24 hours, which is the maximum daily amount for this product take with other drug containing acetaminophen adult has 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause sever skin reactions.
Symptoms may include: skin reddening blisters ras If skin reaction occurs, stop use and seek medical help right away. Sore throat warning: If sore throat is sever, lasts for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. Do not use with any other products containing acetaminophen (prescription or nonprescription).
If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's diseas), or for 2 weeks after stopping the MAOI drugs. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. If you have ever had an allergic reaction to this product or any o its ingredients
🆘 Overdosage ▾
Overdose warning: Taking more than the recommended dose (overdose) may cause serious health problemas including liver damamge. In case of accidental overdose, seek professional assistance or contact a Poison Control Center (1-800-222-1222) immediately. Quick medical attention is critical for adults as well as for children even if ou do not notice any signs or symptoms.
🧪 Active Ingredient ▾
Drug Facts Active ingredients (in each 15 mL dose cup) Acetaminophen 325 mg Dextromethorphan HBr 10 mg Phenylephrine HCl 5 mg
🧪 Inactive Ingredients ▾
Inactive ingredients Citric acid, FD&C Yellow No 6, flavor, glycerin, menthol, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose, xanthan gum
🎯 Purpose ▾
Purpose Pain reliever/fever reducer Cough Suppressant Nasal Decongestant
📄 Ask a Doctor Before Use If ▾
Ask a doctor before use if you have liver disease heart disease high blood pressure diabete thyroid disease trouble urinating due to an enlarged prostate gland cough accompanied by excessive phlegm (mucus) cough that occurs with too much phlegm (mucus) persistent or chronic cough such as occurs with smoking, asthma, or emphysema.
📄 Ask a Doctor or Pharmacist Before Use If ▾
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
📄 When Using This Product ▾
When using this product do not use more than directed (see overdose warning) avoid alcoholic drinks
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if you get nervous, dizzy or sleepless pain, nasal congestion or cough get worse or last more than 5 days (children) or 7 days (adults) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back, or occurs with rash or headache that lasts. These could be signs of a serious condition.
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding, ask a health professional before use.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children.
📄 Other Information ▾
Other information each 15 mL contains: sodium 5 mg store at room temperature 15-30°C (59-86°C) and do not refrigerate
📄 Questions or Comments ▾
Questions or Comments? 1-844-912-4012
📄 Package Label / Principal Display Panel ▾
LABEL
About this NDC listing & data coverage
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |