Antigrip Cold & Cough Gelcaps (HL)

Antigrip by

Drug Labeling and Warnings

Antigrip by is a Otc medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIGRIP COUGH AND COLD- acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, phenylephrine hci0 capsule, gelatin coated 
Pharmadel LLC

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Antigrip Cold & Cough Gelcaps (HL)

Drug Facts

Active ingredients & Purposes

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

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

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

  • 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

  • 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

is taking the blood thinning drug warfarin

When using this product

  • 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

  • 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,

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

  • 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

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

Inactive Ingredients

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

Dist by/ por:

PHARMADEL LLC

New Castle, DE 19720

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

Principal Display Panel

PDP Antigrip

ANTIGRIP  COUGH AND COLD
acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, phenylephrine hci0 capsule, gelatin coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55758-043
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg
PHENYLEPHRINE (UNII: 1WS297W6MV) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE5 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN250 mg
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POVIDONE K30 (UNII: U725QWY32X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITOL (UNII: 506T60A25R)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Product Characteristics
ColorblueScorescore with uneven pieces
ShapeCAPSULE (Oblong Soft gel capsule) Size21mm
FlavorImprint Code SN5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 55758-043-081 in 1 BOX03/24/202412/31/2025
18 in 1 BLISTER PACK; Type 0: Not a Combination Product
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/24/202412/31/2025
Labeler - Pharmadel LLC (030129680)

Revised: 8/2025
 

Trademark Results [Antigrip]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ANTIGRIP
ANTIGRIP
86445838 4909742 Live/Registered
Pharmadel LLC
2014-11-05

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