ACETAMINOPHEN- acetaminophen tablet 
NCS HealthCare of KY, LLC dba Vangard Labs

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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Acetaminophen Tabs 325 mg 8397

DRUG FACTS

Active ingredient (in each tablet)
Acetaminophen 325 mg

Purpose
Pain reliever/fever reducer

Uses

Warnings
Liver Warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children.  Severe liver damage may occur if:

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

Do not use

Ask a doctor before use if the user has liver disease

Ask a doctor or pharmacist before use if the user

is taking the blood thinning drug warfarin

Stop use and ask a doctor if

     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.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away.
(1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

   See overdose warning

 adults and children 12 years and over

children 6 years to under 12 years

children under 6 years
ask a doctor

Other Information

Inactive ingredients
povidone, pregelatinized starch, sodium starch glycolate*, stearic acid
*may contain this ingredient

Questions or comments? call 1-877-290-4008

Manufactured by: Time-Cap Labs, Inc.,

7 Michael Avenue, Farmingdale, NY 11735

340R 1022

PRINCIPAL DISPLAY PANEL- BINGO

Acetaminophen 325mg Tab Bingo Card Label

PRINCIPAL DISPLAY PANEL - UNIT DOSE

PRINCIPAL DISPLAY PANEL - UNIT DOSE
ACETAMINOPHEN 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0615-8397(NDC:49483-340)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeROUNDSize10mm
FlavorImprint Code TCL340
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0615-8397-3930 in 1 BLISTER PACK; Type 0: Not a Combination Product04/26/2021
2NDC:0615-8397-306 in 1 BOX, UNIT-DOSE04/26/2021
25 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:0615-8397-0515 in 1 BLISTER PACK; Type 0: Not a Combination Product11/15/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/15/2011
Labeler - NCS HealthCare of KY, LLC dba Vangard Labs (050052943)
Establishment
NameAddressID/FEIBusiness Operations
NCS HealthCare of KY, LLC dba Vangard Labs050052943repack(0615-8397)

Revised: 1/2023
Document Id: 224b3b3d-1dc4-457c-b6a8-6ee82498daf6
Set id: bb450552-728a-4675-b0a9-0fd2934f6c5e
Version: 5
Effective Time: 20230103
 
NCS HealthCare of KY, LLC dba Vangard Labs