FDA.reportPublic FDA data

Antigrip

Manufacturer
Pharmadel LLC
Effective date
2025-08-21
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:34:52

Label at a glance#

ProductAntigrip Cough and Cold
Active ingredientCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE, ACETAMINOPHEN
Label structure8 sections

Indications and uses

Temporarily relieves common cough and cold symptoms due to minor aches and pain headache runny nose sneezing minor throat and bronchial irritation nasal congestion temporarily reduces fever

Dosage and administration

take each dose with plenty of water Age Dose Adults and children 12 years and over 2 softgels, every 6 hours not to exceed 4 doses in 24 hours children 6 to under 12 years of age 1 softgel, every 4 hours not to exceed 5 doses in 24 hours children under 6 years of age do not use

Label contents#

Full prescribing information#

Active ingredients & Purposes

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients (in each gel capsule)Purposes
Acetaminophen 250 mg ............
Pain reliever/ fever reducer
Chlorpheniramine maleate 2 mg ..........Antihistamine
Dextromethorphan HBr 10 mg.......... Cough suppressant
Phenylephrine HCI 5 mg.......... Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves common cough and cold symptoms due to

  • minor aches and pain
  • headache
  • runny nose
  • sneezing
  • minor throat and bronchial irritation
  • nasal congestion
  • temporarily reduces fever

Warnings

WARNINGS SECTION

Liver Warning: This product contains acetaminophen. Severe liver damage may occur if

  • adult takes more than 4 doses in 24 hours, which is the maximum daily amount for this product
  • child takes more than 5 doses in 24 hours
  • taken with other drugs containing acetaminophen
  • adult has 3 or more alcoholic drinks everyday while using this product

Do not use

OTC - DO NOT USE SECTION

  • 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 prescription monoamine oxidase inhibitors (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 the user

OTC - ASK DOCTOR SECTION

  • is a child with pain from arthritis
  • has liver disease
  • has heart disease
  • has high blood pressure
  • has thyroid disease
  • has diabetes
  • has glaucoma
  • has a breathing problem such as emphysema or chronic bronchitis
  • has difficulty in urination due to enlargement of the prostate gland
  • has a persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • have a cough that is accompanied by excessive phlegm (mucus)
  • are taking sedatives or tranquilizers

Ask a doctor or pharmacist before use if the user

OTC - ASK DOCTOR/PHARMACIST SECTION

is taking the blood thinning drug warfarin

When using this product

OTC - WHEN USING SECTION

  • do not exceed the recommended dosage
  • may cause marked drowsiness
  • may cause excitability, especially in children
  • may cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages while taking this product
  • use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor If

OTC - STOP USE SECTION

  • nervousness, dizziness, or sleeplessness occur
  • pain, cough, or nasal congestion gets worse or lasts 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
  • a cough comes back or occurs with a rash headache that lasts.

These could be signs of a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • take each dose with plenty of water
Age Dose
Adults and children 12 years and over 2 softgels, every 6 hours not to exceed 4 doses in 24 hours
children 6 to under 12 years of age 1 softgel, every 4 hours not to exceed 5 doses in 24 hours
children under 6 years of agedo not use

Other Information

OTHER SAFETY INFORMATION

  • store between 68-77°F (20-25"C)
  • avoid excessive heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

FD&C blue #1, gelatin, glycerin, methylparaben, polyethylene glycol 400, povidone k30, propylene glycol, propylparaben, sorbitol, titanium dioxide, water

Dist by/ por:

OTC - QUESTIONS SECTION

PHARMADEL LLC

New Castle, DE 19720

Questions/ Preguntas? +1-866-359-3478

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP AntigripPDP Antigrip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55758-04355758-043-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORPHENIRAMINE MALEATEV1Q0O9OJ9ZACTIB
TITANIUM DIOXIDE15FIX9V2JPIACT
DEXTROMETHORPHAN HYDROBROMIDE9D2RTI9KYHACTIB
PHENYLEPHRINE1WS297W6MVACTIB
FD&C BLUE NO. 1H3R47K3TBDIACT
GELATIN2G86QN327LIACT
GLYCERINPDC6A3C0OXIACT
ACETAMINOPHEN362O9ITL9DACTIB
POLYETHYLENE GLYCOL 400B697894SGQIACT
POVIDONE K30U725QWY32XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL506T60A25RIACT
METHYLPARABENA2I8C7HI9TIACT
WATER059QF0KO0RIACT
PROPYLPARABENZ8IX2SC1OHIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4d7a8c40-23ff-97bd-e063-6394a90aa6107319e10b-505a-5683-e053-2a91aa0a8d0f2026-03-20WarningsExact identifier
spl set id: 7319e10b-505a-5683-e053-2a91aa0a8d0f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.