Label: ACETAMINOPHEN tablet, extended release
- NDC Code(s): 69842-930-80
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated August 12, 2019
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each geltab)
- Purpose
- Uses
-
Warnings
Liver warning
This product contains acetaminophen. Severe liver damage may occur if you take
- more than 6 geltabs 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
Allergy 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 difficulty swallowing large tablets or capsules. People over 65 may have difficulty swallowing these tablets.
- if you are allergic to acetaminophen or any of the inactive ingredients in this product.
-
Directions
- do not take more than directed (see overdose warning)
adults - take 2 geltabs every 8 hours. Swallow only one geltab at a time.
- take a sip of water before swallowing each geltab and wash each geltab down with water (up to a full 8 oz. glass).
- swallow whole; do not crush, chew, split or dissolve
- do not take more than 6 geltabs in 24 hours
- do not use for more than 10 days unless directed by a doctor
under 18 years of age - ask a doctor
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 650 mg Tablet Bottle Label
CVS
HEALTH™Compare to the active ingredient
in Tylenol® 8HR Arthritis Pain*Geltabs†
8HR Arthritis
Pain Relief
ACETAMINOPHEN
EXTENDED-RELEASE TABLETS, USP 650 mgDO NOT USE WITH OTHER
MEDICINES CONTAINING
ACETAMINOPHENTHIS PACKAGE IS FOR
HOUSEHOLDS WITHOUT
YOUNG CHILDRENPain reliever; Fever reducer
- For the temporary relief
of minor arthritis pain - Lasts up to 8 hours
Use only as directed.
80 GELTABS†
†GELATIN-COATED TABLETSActual Size
- For the temporary relief
-
INGREDIENTS AND APPEARANCE
ACETAMINOPHEN
acetaminophen tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-930 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 650 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white (White to Yellow) Score no score Shape ROUND Size 13mm Flavor Imprint Code 350 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-930-80 80 in 1 BOTTLE; Type 0: Not a Combination Product 12/21/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078569 12/21/2012 Labeler - CVS Pharmacy (062312574) Registrant - Ranbaxy Pharmaceuticals Inc. (937890044) Establishment Name Address ID/FEI Business Operations Ohm Laboratories Inc. 184769029 manufacture(69842-930)