VANQUISH- acetaminophen, aspirin, and caffeine tablet, coated

vanquish by

Drug Labeling and Warnings

vanquish by is a Otc medication manufactured, distributed, or labeled by Strides Pharma Inc, Contract Pharmacal Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Purpose

* nonsteroidal anti-inflammatory drug
Active ingredients; (in each caplet)	Purpose
Acetaminophen 194 mg	Pain reliever
Aspirin 227 mg (NSAID)*	Pain reliever
Caffeine 33 mg	Pain reliever aid

Uses

temporarily relieves minor pain due to 

• headache
• arthritis
• backache
• colds
• menstrual cramps
• muscle aches

Warnings

Reye's syndrome:

Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert:

Aspirin may cause a severe allergic reaction which may include:

• hives
• facial swelling
• asthma (wheezing)
• shock

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.

Liver warning:

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

• more than 8 caplets 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

Stomach bleeding warning:

This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you

• are age 60 or older
• have had stomach ulcers or bleeding problems
• take a blood thinning (anticoagulant) or steroid drug
• take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
• have 3 or more alcoholic drinks every day while using this product
• take more or for a longer time than directed

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 allergic to aspirin or any other pain reliever/fever reducer

Ask a doctor before use if

• you have liver disease
• stomach bleeding warning applies to you
• you have a history of stomach problems, such as heartburn
• you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
• you are taking a diuretic
• you have asthma

Ask a doctor or pharmacist before use if you are

taking a prescription drug for 

• gout
• diabetes
• arthritis

Stop use and ask a doctor if

• an allergic reaction occurs. Seek medical help right away.
• you experience any of the following signs of stomach bleeding
  • feel faint
  • vomit blood
  • have bloody or black stools
  • have stomach pain that does not get better
• pain gets worse or lasts more than 10 days
• redness or swelling is present
• ringing in the ears or loss of hearing occurs
• new symptoms occur

If pregnant or breast-feeding,

ask a health professional before use.

It is especially important not to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

• do not take more than the recommended dose
• drink a full glass of water with each dose
• adults and children 12 years and over: take 2 caplets every 6 hours, not to exceed 8 caplets in 24 hours unless directed by a doctor
• children under 12 years: consult a doctor

Other information

• save carton for full directions and warnings
• store at room temperature

Inactive ingredients

Colloidal Silicon Dioxide, Corn Starch, Hypromellose, Maltodextrin, Microcrystalline Cellulose, Polydextrose, Povidone, Sodium Carboxymethyl Starch, Stearic Acid, Talc, Titanium Dioxide and Triglycerides

Each tablet contains 0.11 mg. of Sodium

Questions or comments?

Call: (844) 94-RELIEF (844-947-3543)

www.vanquishheadacherelief.com

VANQUISH® is a registered trademark of SVADS Holdings SA

Manufactured for Strides Pharma Inc. East Brunswick, NJ 08816

Principal Display Panel

MADE IN USA

VANQUISH®

Effective Headache Relief

Aspirin (NSAID)/Acetaminophen /Caffeine

Pain Reliever/Pain Reliever Aid

100 Analgesic

COATED CAPLETS

Do not use this product if printed safety seal under cap is torn or missing.

EXPIRES

82-375210

Manufactured for Strides Pharma Inc. East Brunswick, NJ 08816

MADE IN USA

VANQUISH®

Effective Headache Relief

Aspirin (NSAID)/Acetaminophen /Caffeine

Pain Reliever/Pain Reliever Aid

100 Analgesic

COATED CAPLETS

Do not use this product if printed safety seal under cap is torn or missing.

EXPIRES

82-220101

VANQUISH® is a registered trademark of SVADS Holdings SA

Manufactured for Strides Pharma Inc. East Brunswick, NJ 08816

MADE IN USA

VANQUISH®

Effective Headache Relief

Aspirin (NSAID)/Acetaminophen /Caffeine

Pain Reliever/Pain Reliever Aid

120 Analgesic

COATED CAPLETS

Do not use this product if printed safety seal under cap is torn or missing.

EXPIRES

82-375210

Manufactured for Strides Pharma Inc. East Brunswick, NJ 08816

-BONUS-

20% MORE!

MADE IN USA

VANQUISH®

Effective Headache Relief

Aspirin (NSAID)/Acetaminophen /Caffeine

Pain Reliever/Pain Reliever Aid

120 Analgesic

COATED CAPLETS

Do not use this product if printed safety seal under cap is torn or missing.

EXPIRES

82-220101

VANQUISH® is a registered trademark of SVADS Holdings SA

Manufactured for Strides Pharma Inc. East Brunswick, NJ 08816

INGREDIENTS AND APPEARANCE

VANQUISH 
acetaminophen, aspirin, and caffeine tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59556-810
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	194 mg
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E)	ASPIRIN	227 mg
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)	CAFFEINE	33 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POLYDEXTROSE (UNII: VH2XOU12IE)
POVIDONE (UNII: FZ989GH94E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	L374
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59556-810-06	1 in 1 CARTON	06/26/2012
1		100 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 59556-810-11	1 in 1 CARTON	06/26/2012
2		120 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	06/26/2012

Labeler - Strides Pharma Inc (078868278)

Registrant - Strides Pharma Global Pte. Ltd. (659220961)

Establishment
Name	Address	ID/FEI	Business Operations
Contract Pharmacal Corporation		057795122	MANUFACTURE(59556-810)