Available Formats

• Active ingredients (in each caplet)

  Acetaminophen 500 mg
  Diphenhydramine HCl 25 mg

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• Purpose

  Pain reliever
  Nighttime sleep-aid

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• Uses

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

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• 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

  • 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
  • in children under 12 years of age
  • 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
  • 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 beverages
  • 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 a serious underlying medical illness.
  • new symptoms occur
  • redness or swelling is present
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days

  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: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

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• Directions

  • do 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 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

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• Other information

  • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
  • see end flap for expiration date and lot number

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• Inactive ingredients

  colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C blue #1 aluminum lake, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, stearic acid, talc, titanium dioxide

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• Principal Display Panel

  For pain with sleeplessness
  Pain Reliever
  Nighttime Sleep-Aid

  Our Family®
  Quality Care Since 1904

  Compare to the
  Active Ingredients
  in Extra Strength
  Tylenol® PM*

  PAIN RELIEVER PM
  ACETAMINOPHEN 500 mg, DIPHENHYDRAMINE HCl 25 mg

  EXTRA STRENGTH

  50 CAPLETS

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

  *This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Extra Strength Tylenol® PM.

  DISTRIBUTED BY:
  NASH FINCH COMPANY ©2004,1996
  NFC BRANDS,
  7600 FRANCE AVE S, MPLS, MN 55435
  www.ourfamilyfoods.com     NF17206
  50844     REV0512E23515

  

  OurFamily44-235

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• INGREDIENTS AND APPEARANCE

  PAIN RELIEVER PM  acetaminophen and diphenhydramine hcl tablet, film coated

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70253-235 Route of Administration ORAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg

  Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4)   CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)   FD&C BLUE NO. 1 (UNII: H3R47K3TBD)   CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)   POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)   POLYVINYL ALCOHOL (UNII: 532B59J990)   POVIDONES (UNII: FZ989GH94E)   STEARIC ACID (UNII: 4ELV7Z65AP)   TALC (UNII: 7SEV7J4R1U)   TITANIUM DIOXIDE (UNII: 15FIX9V2JP)   STARCH, CORN (UNII: O8232NY3SJ)

  Product Characteristics Color BLUE Score no score Shape CAPSULE Size 17mm Flavor Imprint Code 44;235 Contains

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70253-235-08 1 in 1 CARTON 1 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:70253-235-15 1 in 1 CARTON 2 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part343 05/15/1994 07/13/2018

  Labeler - NASH-FINCH COMPANY (006962294)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		832867894	MANUFACTURE(70253-235)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		038154464	PACK(70253-235)

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