Label: PAIN RELIEVER PM- acetaminophen, diphenhydramine hcl tablet, coated
- NDC Code(s): 69607-8630-1
- Packager: WR Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2025
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- Official Label (Printer Friendly)
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Active ingredients (in each caplet)Acetaminophen 500 mg - Diphenhydramine HCL 25 mg
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PurposePain reliever - Nighttime sleep-aid
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Usestemporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness.
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WarningsLiver 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 ...
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Directionsdo not take more than directed (see overdose 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 ...
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Other informationstore between 20-25°C (68-77°F) avoid high humidity and excessive heat
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Inactive ingredientscroscarmellose sodium, FD&C blue #1 aluminum lake, FD&C blue #2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone K30 ...
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Principal Display Panel†Compare to the active ingredient in Extra Strength Tylenol® PM - Extra Strength - Pain Reliever PM - Acetaminophen 500 mg - Pain Reliever - Diphenhydramine HCL 25 mg - Nighttime Sleep Aid - For ages ...
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Package LabelKOLBE & SCHMITT Extra Strength Pain Reliever PM
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INGREDIENTS AND APPEARANCEProduct Information