Label: IBUPROFEN PM- diphenhydramine citrate, ibuprofen tablet, coated
- NDC Code(s): 69607-1970-1
- Packager: WR Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated March 25, 2025
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- Official Label (Printer Friendly)
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Active ingredient (in each caplet)Diphenhydramine citrate 38 mg - ibuprofen 200 mg(NSAID)* *nonsteroidal anti-inflammatory drug
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PurposeNighttime sleep-aid - Pain Reliever
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Usesfor relief of occasional sleeplessness when associated with minor aches and pains - helps you fall asleep and stay asleep
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WarningsAllergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: hives - facial swelling - asthma (wheezing) shock - skin reddening ...
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Directionsdo not take more than directed - adults and childlren 12 years and over: take 2 caplets at bedtime - do not take more than 2 caplets in 24 hours
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Other informationread all warnings and directions before use. Keep carton. store between 20-25°C (68-77°F) avoid excessive heat above 40°C (104°F)
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Inactive ingredientscarnauba wax, corn starch, croscarmellose sodium, FD&C blue #2, hypromellose, microcrystalline cellulose, polydestrose, polyethylene glycol 400, silicon dioxide, stearic acid, titanium dioxide ...
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Principal Display Panel†Compare to the active ingredients in Advil® PM - IbuprofenPM - Ibuprofen 200 mg - Pain reliever (NSAID)* Diphenhydramine citrate 38 mg - Nighttime sleep-aid - Coated caplets** (**Capsules-shaped ...
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Product PackagingKOLBE & SCHMITT Ibuprofen PM
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INGREDIENTS AND APPEARANCEProduct Information