Indications and uses
For the temporary relief of symptoms due to the common cold/ flu: runny nose sneezing nasal congestion minor aches and pain headache and temporarily reduces fever
Antigrip
- Manufacturer
- Pharmadel LLC
- Effective date
- 2024-10-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:32:28
Label at a glance#
ProductAntigrip Extra Strength
Active ingredientCHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN
Label structure9 sections
Dosage and administration
■ adults and children 12 years of age and older: take two (2) tablets fully dissolved in a 4 oz glass of water every 4 hours. Do not exceed 12 tablets in 24 hours or as directed by a doctor. ■ children under 12 years of age: do no use
Contacts and useful links#
Websitewww.pharmadel.com
www.pharmadel.com
www.pharmadel.comLabel contents#
Full prescribing information#
Active ingredients & Purposes
OTC - PURPOSE SECTION
| Active ingredients (in each tablet) | Purposes |
| Acetaminophen 325 mg................... | Pain reliever/ fever reducer |
| Chlorpheniramine maleate 2 mg ........... | Antihistamine |
| Phenylephrine HCl 5 mg ..................... | Nasal decongestant |
Uses
For the temporary relief of symptoms due to the common cold/ flu:
- runny nose
- sneezing
- nasal congestion
- minor aches and pain
- headache
- and temporarily reduces fever
Warnings
Liver Warning: This product contains acetaminophen. Severe liver damage may occur if you take
- more than 12 tablets in 24 hours, which is the maximum daily amount for this product
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash. If a skin reaction occurs, stop use and seek medical help right away.
Sore throat warning: If sore throat is severe, persists for more than 2 days, and is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Do not use
- with any other drug 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 disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask your doctor or pharmacist before taking this product
Ask a doctor before use if you have
- liver disease
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- difficulty in urination due to enlargement of the prostate gland
Ask a doctor or pharmacist before use if you are
- taking the blood thinning drug warfarin
- taking sedatives or tranquilizers
When using this product
- do not exceed the recommended dosage
- may cause drowsiness
- may cause excitability, especially in children
- avoid alcoholic beverages while taking this product
- use caution when driving a motor vehicle or operating machinery
Stop use and ask a doctor if
- nervousness, dizziness, or sleeplessness occurs
- pain or nasal congestion persists for more than 7 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present
- new symptoms occur
If pregnant or breastfeeding,
ask a health professional before use.
Keep out of reach of children.
In case of an accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Directions
■ adults and children 12 years of age and older: take two (2) tablets fully dissolved in a 4 oz glass of water every 4 hours. Do not exceed 12 tablets in 24 hours or as directed by a doctor.
■ children under 12 years of age: do no use
Other information
- each tablet contains: potassium 10mg, sodium 246mg
- store below 77°F (25°C) and a dry place
Inactive ingredients
acesulfame potassium, anhydrous citric acid, FD&C red #40, polysorbate 80, povidone k-30, simethicone, sodium benzoate, sodium bicarbonate, strawberry flavor, sucralose, water.
Questions or comments?
+1-866-359-3478 (M-F) 9 AM to 5 PM EST or www.pharmadel.com
Dist. by:
Pharmadel LLC.
New Castle, DE 19720
Principle Display Panel
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 2691098 | acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine HCl 5 MG Effervescent Oral Tablet | PSN | 1 |
| 2691098 | acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet | SCD | 1 |
| 2691098 | APAP 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet | SY | 1 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CHLORPHENIRAMINE Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
| PHENYLEPHRINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55758-500-72 | AntigripExtra Strength | 36 in 1 CARTON | TABLET, EFFERVESCENT | 36 | 1 | |
| 55758-500-72 | AntigripExtra Strength | 2 in 1 POUCH | TABLET, EFFERVESCENT | 2 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Antigrip Extra Strength
- Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl
- FD&C RED NO. 40
- CHLORPHENIRAMINE MALEATE
- CHLORPHENIRAMINE
- WATER
- ACESULFAME POTASSIUM
- ANHYDROUS CITRIC ACID
- POLYSORBATE 80
- SILICON DIOXIDE
- SUCRALOSE
- POVIDONE K30
- SODIUM BENZOATE
- SODIUM BICARBONATE
- PHENYLEPHRINE HYDROCHLORIDE
- PHENYLEPHRINE
- ACETAMINOPHEN
- DIMETHICONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55758-500 | 55758-500-72 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| CHLORPHENIRAMINE MALEATE | V1Q0O9OJ9Z | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ACESULFAME POTASSIUM | 23OV73Q5G9 | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| POVIDONE K30 | U725QWY32X | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SODIUM BICARBONATE | 8MDF5V39QO | IACT |
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | ACTIB |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| DIMETHICONE | 92RU3N3Y1O | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Antigrip Extra Strength | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL | Pharmadel LLC | 25a26adf-fd90-bf57-e063-6294a90a4073 | 2024-10-29 | Warnings | 55758-500-72 55758-500 55758050072 25a26adf-fd91-bf57-e063-6294a90a4073 25a26adf-fd90-bf57-e063-6294a90a4073 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.