regular strength pain reliever
4417b3dd-5560-4828-b656-f7c7788744c3
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Purpose
Pain reliever/fever reducer
Description
Drug Facts
Medication Information
Warnings
Liver warning
This product contains acetaminophen. The maximum daily dose of this product is 10 softgels (3,250 mg) in 24 hours for adults or 5 softgels (1,625 mg) in 24 hours for children. Severe liver damage may occur if
- adult takes more than 4,000 mg of acetaminophen in 24 hours
- child takes more than 5 doses in 24 hours, which is the maximum daily amount
- taken with other drugs containing acetaminophen
- adult has 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.
Uses
- temporarily relieves minor aches and pains due to:
-
- headache
- muscular aches
- backache
- minor pain of arthritis
- the common cold
- toothache
- premenstrual and menstrual cramps
- temporarily reduces fever
Purpose
Pain reliever/fever reducer
Directions
- do not take more than directed (see Overdose warning)
|
adults and children 12 years and over |
|
|
children 6-11 years |
|
|
children under 6 years |
ask a doctor |
Other Information
- store at room temperature 15°-30°C (59°-86°F)
Inactive Ingredients
FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution and white edible ink
Description
Drug Facts
Section 42229-5
Drug Facts
Section 50565-1
Keep out of reach of children.
Section 50568-5
Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin
Section 50569-3
Ask a doctor before use if the user has liver disease
Section 53414-9
If pregnant or breast-feeding, ask a health professional before use.
Do Not Use
- 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
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.
Questions Or Comments?
Call: 1-888-309-9030
Stop Use and Ask A Doctor If
- pain gets worse or lasts more than 10 days in adults
- pain gets worse or lasts more than 5 days in children under 12 years
- 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.
Active Ingredient (in Each Softgel)
Acetaminophen 325 mg
Principal Display Panel Bottle Label 20ct
DG Regular Strength Pain Reliever 20 Softgels
Acetaminophen 325mg
NDC 51013-173-15
*Compare to the active ingredient in TYLENOL® Regular Strength
Principal Display Panel Bottle Label 24ct
DG Regular Strength Pain Reliever 24 Softgels
Acetaminophen 325mg
NDC 51013-173-43
*Compare to the active ingredient in TYLENOL® Regular Strength
Principal Display Panel Bottle Label 40ct
DG Regular Strength Pain Reliever 40 Softgels
Acetaminophen 325mg
NDC 51013-173-25
*Compare to the active ingredient in TYLENOL® Regular Strength
Structured Label Content
Warnings
Liver warning
This product contains acetaminophen. The maximum daily dose of this product is 10 softgels (3,250 mg) in 24 hours for adults or 5 softgels (1,625 mg) in 24 hours for children. Severe liver damage may occur if
- adult takes more than 4,000 mg of acetaminophen in 24 hours
- child takes more than 5 doses in 24 hours, which is the maximum daily amount
- taken with other drugs containing acetaminophen
- adult has 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.
Uses
- temporarily relieves minor aches and pains due to:
-
- headache
- muscular aches
- backache
- minor pain of arthritis
- the common cold
- toothache
- premenstrual and menstrual cramps
- temporarily reduces fever
Purpose
Pain reliever/fever reducer
Directions
- do not take more than directed (see Overdose warning)
|
adults and children 12 years and over |
|
|
children 6-11 years |
|
|
children under 6 years |
ask a doctor |
Other Information (Other information)
- store at room temperature 15°-30°C (59°-86°F)
Inactive Ingredients (Inactive ingredients)
FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution and white edible ink
Section 42229-5 (42229-5)
Drug Facts
Section 50565-1 (50565-1)
Keep out of reach of children.
Section 50568-5 (50568-5)
Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin
Section 50569-3 (50569-3)
Ask a doctor before use if the user has liver disease
Section 53414-9 (53414-9)
If pregnant or breast-feeding, ask a health professional before use.
Do Not Use (Do not use)
- 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
Overdose Warning (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.
Questions Or Comments? (Questions or comments?)
Call: 1-888-309-9030
Stop Use and Ask A Doctor If (Stop use and ask a doctor if)
- pain gets worse or lasts more than 10 days in adults
- pain gets worse or lasts more than 5 days in children under 12 years
- 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.
Active Ingredient (in Each Softgel) (Active ingredient (in each softgel))
Acetaminophen 325 mg
Principal Display Panel Bottle Label 20ct (PRINCIPAL DISPLAY PANEL - Bottle Label 20ct)
DG Regular Strength Pain Reliever 20 Softgels
Acetaminophen 325mg
NDC 51013-173-15
*Compare to the active ingredient in TYLENOL® Regular Strength
Principal Display Panel Bottle Label 24ct (PRINCIPAL DISPLAY PANEL - Bottle Label 24ct)
DG Regular Strength Pain Reliever 24 Softgels
Acetaminophen 325mg
NDC 51013-173-43
*Compare to the active ingredient in TYLENOL® Regular Strength
Principal Display Panel Bottle Label 40ct (PRINCIPAL DISPLAY PANEL - Bottle Label 40ct)
DG Regular Strength Pain Reliever 40 Softgels
Acetaminophen 325mg
NDC 51013-173-25
*Compare to the active ingredient in TYLENOL® Regular Strength
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T11:56:56.454648 · Updated: 2026-03-14T22:55:45.140912