NDC | 0573-0199-01, 0573-0199-03, 0573-0199-11, 0573-0199-21, 0573-0199-22 |
Set ID | b1e29c19-fe03-4d2b-b966-0adf4eb4b4cf |
Category | HUMAN OTC DRUG LABEL |
Packager | Wyeth Consumer Healthcare LLC |
Generic Name | |
Product Class | alpha-1 Adrenergic Agonist |
Product Number | |
Application Number | NDA022565 |
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
Allergy alert
Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
- hives
- facial swelling
- asthma (wheezing)
- shock
- skin reddening
- rash
- blisters
If an allergic reaction occurs, stop use and seek medical help right away.
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
Heart attack and stroke warning
NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.
Do not use
- in children under 12 years of age because this product contains too much medication for children under this age
- if you have ever had an allergic reaction to any other pain reliever/fever reducer
- right before or after heart surgery
- 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 a doctor or pharmacist before taking this product
Ask a doctor before use if
- stomach bleeding warning applies to you
- you have problems or serious side effects from taking pain relievers or fever reducers
- you have a history of stomach problems, such as heartburn
- you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, thyroid disease, diabetes, have trouble urinating due to an enlarged prostate gland, or had a stroke
- you are taking a diuretic
Ask a doctor or pharmacist before use if you are
- under a doctor's care for any serious condition
- taking any other product that contains phenylephrine or any other nasal decongestant
- taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
- taking any other drug
Stop use and ask a doctor if
- 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
- you have symptoms of heart problems or stroke:
- chest pain
- trouble breathing
- weakness in one part or side of body
- slurred speech
- leg swelling
- pain gets worse or lasts more than 7 days
- fever gets worse or lasts more than 3 days
- nasal congestion lasts for more than 7 days
- symptoms continue or get worse
- redness or swelling is present in the painful area
- you get nervous, dizzy, or sleepless
- any new symptoms appear
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DOSAGE & ADMINISTRATION
Directions
- do not take more than directed
- adults and children 12 years of age and over:
- take 1 tablet every 4 hours while symptoms persist.
- do not use more than 6 tablets in any 24-hour period unless directed by a doctor
- children under 12 years of age: do not use because this product contains too much medication for children under this age
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients
acesulfame potassium, artificial flavor, carnauba wax, colloidal silicon dioxide, corn starch, croscarmellose sodium, glycerin, hypromellose, lactic acid, lecithin, maltodextrin, medium-chain triglycerides, microcrystalline cellulose, pharmaceutical ink, polydextrose, polyvinyl alcohol, pregelatinized starch, propyl gallate, sodium lauryl sulfate, stearic acid, sucralose, synthetic iron oxide, talc, titanium dioxide, triacetin, xanthan gum
- QUESTIONS
- PRINCIPAL DISPLAY PANEL - 1 Tablet Pouch
- PRINCIPAL DISPLAY PANEL - 50 Pouch Tray
- PRINCIPAL DISPLAY PANEL - 10 Tablet Blister Pack
- PRINCIPAL DISPLAY PANEL - 20 Tablet Blister Pack Carton
- Principal Display Panel - 30 Tablet Blister Pack Carton
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INGREDIENTS AND APPEARANCE
ADVIL SINUS CONGESTION AND PAIN
ibuprofen, phenylephrine hydrochloride tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0199 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength ACESULFAME POTASSIUM (UNII: 23OV73Q5G9) CARNAUBA WAX (UNII: R12CBM0EIZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) MALTODEXTRIN (UNII: 7CVR7L4A2D) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYDEXTROSE (UNII: VH2XOU12IE) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) PROPYL GALLATE (UNII: 8D4SNN7V92) SODIUM LAURYL SULFATE (UNII: 368GB5141J) STEARIC ACID (UNII: 4ELV7Z65AP) SUCRALOSE (UNII: 96K6UQ3ZD4) FERRIC OXIDE RED (UNII: 1K09F3G675) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color BROWN (tan) Score no score Shape OVAL Size 15mm Flavor Imprint Code 1200;P10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-0199-11 10 in 1 CARTON 07/01/2015 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0573-0199-21 20 in 1 CARTON 07/01/2015 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0573-0199-01 50 in 1 TRAY 07/01/2015 3 1 in 1 POUCH; Type 0: Not a Combination Product 4 NDC:0573-0199-22 30 in 1 CARTON 11/02/2015 4 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:0573-0199-03 3000 in 1 CARTON 07/01/2015 5 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA022565 07/01/2015 Labeler - Wyeth Consumer Healthcare LLC (828831730) Registrant - Pfizer Inc (113480771) Establishment Name Address ID/FEI Business Operations Wyeth Pharmaceuticals Company 829390975 ANALYSIS(0573-0199) , LABEL(0573-0199) , MANUFACTURE(0573-0199) , PACK(0573-0199) Establishment Name Address ID/FEI Business Operations Wyeth Consumer Healthcare LLC 828831730 ANALYSIS(0573-0199) , MANUFACTURE(0573-0199)