Label: RIGHT REMEDIES PAIN RELIEF EXTRA STRENGTH CAPLET- acetaminophen tablet, coated
- NDC Code(s): 70692-150-05, 70692-150-20, 70692-150-31, 70692-150-44
- Packager: Strive Pharmaceuticals Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 21, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient (in each caplet)
- Purpose
- Uses
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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 productAllergy Alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
• skin reddening • blisters • rash
If a skin reaction occurs, stop use and seek medical help right away.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
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.Stop use and ask a doctor if • pain gets worse or lasts more than 10 days • fever gets worse or lasts more than 3 days • new symptoms occur • redness or swelling is present.
These could be signs of a serious condition.If pregnant or breast-feeding, ask a health professional before use.
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Directions
Do not take more than directed. See overdose warning
adult & children
12 years of age
and over• take 2 caplets every 6 hours while symptoms last
• do not take more than 6 caplets in 24 hours unless directed by a doctor
• do not take more than 10 days, unless directed by a doctor
children under 12 years of age
• ask a doctor - Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
*compare to the active ingredient of Extra Strength Tylenol®
TAMPER EVIDENT. DO NOT USE IF IMPRINTED SEAL UNDER CAP IS BROKEN OR MISSING FROM BOTTLE
Distributed by: Strive Pharmaceuticals inc. East Brunswick, NJ 08816
Product of India
Packaged & Quality Assured in USA
READ AND KEEP OUTER PACKAGE FOR COMPLETE PRODUCT INFORMATION
*This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division., owner of the registered trademark Tylenol® Extra Strength Caplets.
REV.00- 102022
- Packaging
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INGREDIENTS AND APPEARANCE
RIGHT REMEDIES PAIN RELIEF EXTRA STRENGTH CAPLET
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70692-150 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) POVIDONE K30 (UNII: U725QWY32X) WATER (UNII: 059QF0KO0R) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) STARCH, CORN (UNII: O8232NY3SJ) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score no score Shape capsule Size 18mm Flavor Imprint Code S150 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70692-150-05 50 in 1 PACKAGE; Type 0: Not a Combination Product 07/20/2022 2 NDC:70692-150-20 200 in 1 BOTTLE; Type 0: Not a Combination Product 07/20/2022 3 NDC:70692-150-44 1 in 1 CARTON 11/21/2023 3 40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:70692-150-31 300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 07/20/2022 Labeler - Strive Pharmaceuticals Inc. (080028013)