DrugCite

UP AND UP ACETAMINOPHEN PM - acetaminophen and diphenhydramine hydrochloride tablet, film coated 
Target Corporation

Target Corporation Acetaminophen PM Drug Facts

Active ingredients (in each caplet)

Acetaminophen 500 mg

Diphenhydramine HCl 25 mg

Purpose

Pain reliever

Nighttime sleep aid

Uses

temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness

Warnings

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

Do not use

in children under 12 years of age
with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
with any other product containing diphenhydramine, even one used on skin
if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

liver disease
a breathing problem such as emphysema or chronic bronchitis
trouble urinating due to an enlarged prostate gland
glaucoma

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin
taking sedatives or tranquilizers

When using this product

drowsiness will occur
avoid alcoholic drinks
do not drive a motor vehicle or operate machinery

Stop use and ask a doctor if

sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.
pain gets worse or lasts more than 10 days
fever gets worse or lasts more than 3 days
redness or swelling is present
new symptoms occur

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.

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 Liver warning)

Adults and children 12 years and over:

take 2 caplets at bedtime
do not take more than 2 caplets of this product in 24 hours
 
 

Children under 12 years: do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Inactive ingredients

carnauba wax, colloidal silicon dioxide, croscarmellose sodium, FD&C blue no. 1 aluminum lake, FD&C blue no. 2 aluminum lake, hypromellose, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, stearic acid, titanium dioxide

Questions?

Call 1-800-910-6874

Package/Label Principal Display Panel

acetaminophen pm

extra strength

acetaminophen 500 mg

diphenhydramine HCl 25 mg

Compare to active ingredients in Extra Strength Tylenol® PM

NIGHT

see new warnings information

pain reliever, nighttime sleep aid

for pain with sleeplessness

# CAPLETS {Replace “#” with number of tablets in package}

SHOWN ACTUAL SIZE ABOVE

Acetaminophen PM Carton Image 1
Acetaminophen PM Carton Image 2

UP AND UP ACETAMINOPHEN PM 
acetaminophen, diphenhydramine hcl  tablet, film coated
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 11673-751
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 500 mg
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
CARNAUBA WAX  
SILICON DIOXIDE  
CROSCARMELLOSE SODIUM  
HYPROMELLOSES  
CELLULOSE, MICROCRYSTALLINE  
POLYETHYLENE GLYCOLS  
POLYSORBATE 80  
POVIDONE  
STEARIC ACID  
TITANIUM DIOXIDE  
Product Characteristics
Color BLUE Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code L751
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 11673-751-71 1  In 1 CARTON contains a BOTTLE
1 50  In 1 BOTTLE This package is contained within the CARTON (11673-751-71)
2 11673-751-78 1  In 1 CARTON contains a BOTTLE
2 100  In 1 BOTTLE This package is contained within the CARTON (11673-751-78)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part343 02/24/2012

Labeler - Target Corporation (006961700)
Revised: 08/2012Target Corporation