ANACIN- asprin and caffeine tablet 
Insight Pharmaceuticals LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Anacin - 63736-200

ANACIN- asprin and caffeine tablet Insight Pharmaceuticals

ANACIN®

Drug Facts

Active ingredients (per tablet)

Aspirin (NSAID)* 400 mg
Caffeine 32 mg

* nonsteroidal anti- inflammatory drug

Purposes

Pain reliever
Pain reliever aid

Uses

temporarily relieves minor aches and pains due to

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:

Stomach bleeding warning

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

Do not use 

if you have ever had an allergic reaction to any other pain reliever/fever reducer

Ask a doctor before use if

  • 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 diabetes, gout, or 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
  • new symptoms occur
  • ringing in the ears or loss of hearing occurs
  • redness or swelling is present
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days

Caffeine warning

The recommended dose of this product contains about as much caffeine as a cup of coffee. Limit the use of caffeine-containing medications, foods or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heart beat.

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.

Overdose warning

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Other information

Keep carton for full drug facts and warnings.

Store at 15 – 25°C (59– 77°F). Protect from moisture.

Inactive ingredients

corn starch, hypromellose, microcrystalline cellulose, polyethylene glycol, sodium lauryl sulfate

Questions?

1-800-344-7239 anacin.com

PRINCIPAL DISPLAY PANEL

ANACIN®

Aspirin (NSAID) Pain Reliever / Caffeine Pain Reliever Aid

100 COATED TABLETS

ANACIN®

Aspirin (NSAID) Pain Reliever / Caffeine Pain Reliever Aid
100 COATED TABLETS

ANACIN 
asprin and caffeine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-200
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN400 mg
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE32 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
STARCH, CORN (UNII: O8232NY3SJ)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize10mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-200-041 in 1 BOX06/25/200906/30/2023
14 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:63736-200-931 in 1 BOX06/25/2009
2300 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:63736-200-301 in 1 BOX06/25/200906/30/2023
330 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:63736-200-501 in 1 BOX06/25/2009
450 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:63736-200-901 in 1 BOX06/25/2009
5100 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:63736-200-911 in 1 BOX06/25/200906/30/2023
6130 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:63736-200-92125 in 1 BOX06/25/2009
71 in 1 POUCH; Type 0: Not a Combination Product
8NDC:63736-200-95750 in 1 BOX06/25/200906/30/2023
81 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34306/25/2009
Labeler - Insight Pharmaceuticals LLC (055665422)

Revised: 7/2020
Document Id: 11bd624d-b3d5-4ea4-ae24-705364eb2603
Set id: 51ab0ee3-3c94-424d-a30a-2d6c14e3d8ff
Version: 6
Effective Time: 20200702
 
Insight Pharmaceuticals LLC