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

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]

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

For the temporary relief of the common cold symptoms:

• minor aches & pains
• headache
• runny nose
• sneezing
• cough due to minor throat and bronchial irritation
• nasal & sinus congestion
• minor throat and bronchial irritation
• nasal congestion
• temporarily reduces fever

Warnings

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

• more than 12 gelcaps 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

Do not use

• with any other drug containing acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
• if you are now taking prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or 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
• have heart disease
• have high blood pressure
• have thyroid disease
• have diabetes
• have glaucoma
• have a breathing problem such as emphysema or chronic bronchitis
• have difficulty in urination due to enlargement of the prostate gland
• have a persistent or chronic cough 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 you are

• taking the blood thinning drug warfariin

When using this product

• do not exceed the recommended dosage
• may cause marked 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, cough, or nasal congestion gets worse or lasts more than 7 days
• 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

• adults and children 12 years and over: take two (2) capsules with water every 4 hours. Do not exceed 12 gelcaps in 24 hours
• children under 12 years of age: do not use

Other Information

• store between 68-77°F (20-25"C)
• avoid excessive heat
• do not use if blister foil is punctured or torn

Inactive Ingredients

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

Questions & comments?

+1-866-359-3478 (M·F) 9 AM to 5 PM EST or www.pharmadel.com

Principal Display Panel

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-043
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
PHENYLEPHRINE (UNII: 1WS297W6MV) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE	5 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	250 mg

Inactive Ingredients
Ingredient Name	Strength
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)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Characteristics
Color	blue	Score	score with uneven pieces
Shape	CAPSULE (Oblong Soft gel capsule)	Size	21mm
Flavor		Imprint Code	SN5
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-043-08	1 in 1 BOX	03/24/2024
1		8 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	03/24/2024

Labeler - Pharmadel LLC (030129680)