Label: MENSTRUAL RELIEF- acetaminophen,caffeine,pyrilamine tablet
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated October 23, 2013
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- Active Ingredient
SEE BOTTLE FOR ADDITIONAL WARNINGS AND PRODUCT INFORMATION.
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 drug 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
- 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 as a cup of coffee.
Stop use and ask a doctor if:
- 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
If pregnant or breast feeding ask a health professional before use.
- Keep out of reach of children.
- Other Information
- Inactive Ingredients
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76168-064 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) STARCH, CORN (UNII: O8232NY3SJ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SHELLAC (UNII: 46N107B71O) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) Product Characteristics Color WHITE Score no score Shape CAPSULE Size 17mm Flavor Imprint Code CH Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76168-064-03 20 in 1 BOTTLE 1 1 in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 05/01/2013 Labeler - Velocity Pharma (962198409) Registrant - Velocity Pharma (962198409)