Drug Facts

Active Ingredient (in each tablet)

Acetaminophen 500 mg

Purpose

Pain reliever/ Fever reducer

Uses

Temporarily reduces fever and relieves minor aches and pains due to:

headache
muscular aches
backache
minor pain of arthritis
the common cold
toothache
premenstrual and menstrual cramps

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

more than 4,000 mg of acetaminophen in 24 hours
with other drugs containing acetaminophen
3 or more alcoholic drinks every day while using this product

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.

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 acetaminophen or any of the inactive ingredients in this product

Ask a doctor before use if you have liver disease

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Stop use and ask a doctor if 

pain gets worse or lasts more than 10 days
fever gets worse or lasts more than 3 days 
new symptoms occur 
redness or swelling is present

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

do not take more than directed (see overdose warning)

adults and children 12 years and over:

• take 2 tablets every 6 hours while symptoms last

• do not take more than 6 tablets in 24 hours, unless directed by a doctor

• do not take for more than 10 days unless directed by a doctor

children under 12 years: ask a doctor

Other Information

store in a dry place at 15° – 30°C (59° – 86°F).

Povidone, pregelatinized starch, sodium starch glycolate, stearic acid

Questions or comments?

Call 1-800-231-4670

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

Distributed by:

MAJOR® PHARMACEUTICALS
Indianapolis, IN 46268

*This product is not manufactured or distributed by Kenvue Inc., owner of the registered trademark Tylenol®.

HOW SUPPLIED

Acetaminophen Tablets 500 mg

NDC: 71335-1536-1: 20 Tablets in a BOTTLE
NDC: 71335-1536-2: 15 Tablets in a BOTTLE
NDC: 71335-1536-3: 40 Tablets in a BOTTLE
NDC: 71335-1536-4: 100 Tablets in a BOTTLE
NDC: 71335-1536-5: 30 Tablets in a BOTTLE
NDC: 71335-1536-6: 45 Tablets in a BOTTLE
NDC: 71335-1536-7: 50 Tablets in a BOTTLE
NDC: 71335-1536-8: 60 Tablets in a BOTTLE
NDC: 71335-1536-9: 90 Tablets in a BOTTLE
NDC: 71335-1536-0: 250 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Acetaminophen Tablets 500 mg

ACETAMINOPHEN
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71335-1536(NDC:0904-6730)
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
POVIDONE K30 (UNII: U725QWY32X)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	12mm
Flavor		Imprint Code	54;27
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71335-1536-1	20 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
2	NDC:71335-1536-2	15 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
3	NDC:71335-1536-3	40 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
4	NDC:71335-1536-4	100 in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
5	NDC:71335-1536-5	30 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2020
6	NDC:71335-1536-6	45 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
7	NDC:71335-1536-7	50 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
8	NDC:71335-1536-8	60 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
9	NDC:71335-1536-9	90 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024
10	NDC:71335-1536-0	250 in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	09/12/2018

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)