ASPIRIN 325 MG EC- aspirin tablet 
Bryant Ranch Prepack

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ASPIRIN 325 MG EC TABLET

Drug Facts

Aspirin USP, 325 mg (NSAID)*

*nonsteroidal anti-inflammatory drug

Pain Reliever/Fever Reducer

temporarily relieves

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

Drug Facts continued on back of label

Do not use if you have ever had an allergic reaction to any other pain reliever/fever reducer

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

Stop use and ask a doctor if

• feel faint

• vomit blood

• have bloody or black stools

• have stomach pain that does not get better

These could be sings of a serious condition

If pregnant or breast-feeding, ask a health professional before use. It is especially imporant 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.

Directions

DRINK A FULL GLASS OF WATER WITH EACH DOSE

Other information

Inactive ingredients

croscarmellose sodium, D&C yellow #10 (Al-lake), FD&C yellow #6 (Al-lake), HPMC, methacrylic acid copolymer, polyethylene glycol, propylene glycol, povidone, sodium lauryl sulfate, starch, stearic acid, talc, titanium dioxide

Questions or comments?

Questions or comments ? call 516-341-0666, 8:30 am - 4:30 pm ET, Monday - Friday

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

*Reliable 1 Laboratories LLC is not affiliated with the owner of the trademark Ecotrin®.

Distributed by: Reliable 1 Laboratories LLC, Valley Stream, NY 11580

www.reliable1labs.com

HOW SUPPLIED

NDC: 71335-1800-1: 30 Tablets in a BOTTLE

NDC: 71335-1800-2: 60 Tablets in a BOTTLE

NDC: 71335-1800-3: 100 Tablets in a BOTTLE

NDC: 71335-1800-4: 90 Tablets in a BOTTLE

NDC: 71335-1800-5: 20 Tablets in a BOTTLE

NDC: 71335-1800-6: 45 Tablets in a BOTTLE

NDC: 71335-1800-7: 120 Tablets in a BOTTLE

NDC: 71335-1800-8: 7 Tablets in a BOTTLE

Aspirin E.C 325mg Tablet

Label
ASPIRIN 325 MG EC 
aspirin tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-1800(NDC:69618-015)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN325 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
METHACRYLIC ACID (UNII: 1CS02G8656)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STARCH, CORN (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TALC (UNII: 7SEV7J4R1U)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize10mm
FlavorImprint Code AP;110
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-1800-130 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
2NDC:71335-1800-260 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
3NDC:71335-1800-3100 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
4NDC:71335-1800-490 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
5NDC:71335-1800-520 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
6NDC:71335-1800-645 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
7NDC:71335-1800-7120 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
8NDC:71335-1800-87 in 1 BOTTLE; Type 0: Not a Combination Product02/24/2022
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01311/01/2015
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-1800) , RELABEL(71335-1800)

Revised: 1/2024
Document Id: 83bb67f7-02d2-497d-8252-1da872534759
Set id: 9d0449d2-c0c6-4e74-931b-35dc62584028
Version: 101
Effective Time: 20240125
 
Bryant Ranch Prepack