Label: MIDOL COMPLETE- acetaminophen, caffeine, and pyrilamine maleate tablet
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NDC Code(s):
85237-1841-1,
85237-1841-2,
85237-1841-3,
85237-1841-4, view more85237-1841-5
- Packager: Select Consumer Group
- This is a repackaged label.
- Source NDC Code(s): 0280-8005
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 27, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
Liver warning
This product contains acetaminophen. Severe liver damage may occur if you take
- more than 6 caplets in 24 hours, which is the maximum daily amount for this product
- 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.
- 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
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
Ask a doctor or pharmacist before use if you are
- taking the blood thinning drug warfarin
- taking sedatives or tranquilizers
When using this product
- you may get drowsy
- avoid alcoholic drinks
- excitability may occur, especially in children
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
- limit the use of caffeine-containing medications, foods, or beverages because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heartbeat. The recommended dose of this product contains about as much caffeine as a cup of coffee.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 30 pouches of 2 caplets
- Package / Label Principal Display 2 caplet pack
- Principal Package / Label display panel 4 caplets Multipack
- Package / Label Principal DIsplay Panel 25 Pouches of 2 caplets
- Package / Label Principal Display Panel 20 pack of 2 caplets
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INGREDIENTS AND APPEARANCE
MIDOL COMPLETE
acetaminophen, caffeine, and pyrilamine maleate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85237-1841(NDC:0280-8005) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 60 mg PYRILAMINE MALEATE (UNII: R35D29L3ZA) (PYRILAMINE - UNII:HPE317O9TL) PYRILAMINE MALEATE 15 mg Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) HYPROMELLOSES (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SHELLAC (UNII: 46N107B71O) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) Product Characteristics Color white Score no score Shape OVAL (oblong) Size 17mm Flavor Imprint Code MIDOL Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85237-1841-1 1 in 1 BLISTER PACK 02/10/2014 1 2 in 1 POUCH; Type 0: Not a Combination Product 2 NDC:85237-1841-2 2 in 1 BLISTER PACK 02/10/2014 2 2 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:85237-1841-3 20 in 1 BOX, UNIT-DOSE 02/10/2014 3 2 in 1 POUCH; Type 0: Not a Combination Product 4 NDC:85237-1841-4 25 in 1 BOX, UNIT-DOSE 02/10/2014 4 2 in 1 POUCH; Type 0: Not a Combination Product 5 NDC:85237-1841-5 30 in 1 BOX, UNIT-DOSE 02/10/2014 5 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M027 02/10/2014 Labeler - Select Consumer Group (119185084) Registrant - Select Consumer Group (119185084) Establishment Name Address ID/FEI Business Operations Select Consumer Group 119185084 repack(85237-1841)





