NDC | 60683-129-13, 60683-129-33 |
Set ID | 6d7c6dda-5268-4169-901d-cd3d750ecce1 |
Category | HUMAN OTC DRUG LABEL |
Packager | Lab Safety Supply, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART343 |
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 8 tablets in 24 hours, which is the maximum daily amount
- 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.
- for more than 10 days for pain unless directed by a doctor
- for more than 3 days for fever unless directed by a doctor
Stop using and ask a doctor if
- symptoms do not improve
- new symptoms occur
- pain or fever persists or gets worse
- redness or swelling is present
- Directions
- Other information
- Inactive ingredients
- Questions or comments? 1-800-356-0783
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PRINCIPAL DISPLAY PANEL
175R LSS XS Non Aspirin 500 mg Label
Rapid Comfort™
Extra Strength
Non-Aspirin
Acetaminophen 500 mg
Easy to Swallow
Film-Coated Tablets
Pull to Open
Compare active ingredient to:
Extra Strength Tylenol®
Registered Trademark of McNeil Consumer Products
See new warnings information
100 Tablets (50 x 2s)
Tamper-Evident Unit Dose Packets
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INGREDIENTS AND APPEARANCE
RAPID COMFORT EXTRA STRENGTH NON ASPIRIN
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60683-129 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 CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) HYPROMELLOSES (UNII: 3NXW29V3WO) MALTODEXTRIN (UNII: 7CVR7L4A2D) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 12mm Flavor Imprint Code FR;33 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60683-129-33 50 in 1 BOX, UNIT-DOSE 1 2 in 1 PACKET 2 NDC:60683-129-13 250 in 1 BOX, UNIT-DOSE 2 2 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 10/14/2011 Labeler - Lab Safety Supply, Inc. (042851410)