Label: CVS HEALTH EXTRA STRENGTH ACETAMINOPHEN SOFTGELS- acetaminophen capsule, liquid filled
- NDC Code(s): 69842-636-40
- Packager: CVS Pharrmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each softgel)
- Purpose
- Uses
-
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 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
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Overdose warning
-
Directions
do not take more than directed (see Overdose warning)
Adults and children 12 years and over ■ take 2 softgels every 6 hours while
symptoms last
■ do not take more than 6 softgels in
24 hours unless directed by a doctor
■ do not use for more than 10 days
unless directed by a doctorchildren under
12 yearsask a doctor - Other information
- Inactive ingredients
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
CVS Health
Compare to the active ingredient
in Tylenol® Extra Strength*
Liquid Gels**
EXTRA STRENGTH
Acetaminophen USP 500mgPain Reliever; Fever reducer
Aspirin free
40 SOFTGELS**
**Liquid filled capsulesTAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSINGThis product is not manufactured
or distributed by McNeil Consumer
Healthcare, owner of the
registered trademark Tylenol®
Extra Strength.Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2019 CVS/pharmacy
CVS.com® 1-800-SHOP CVS
Made in India
V-35257
#960109 -
INGREDIENTS AND APPEARANCE
CVS HEALTH EXTRA STRENGTH ACETAMINOPHEN SOFTGELS
acetaminophen capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-636 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 GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) POVIDONE K30 (UNII: U725QWY32X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color red (transparent) Score no score Shape OVAL Size 23mm Flavor GRAPE Imprint Code 710 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-636-40 40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 06/05/2019 Labeler - CVS Pharrmacy (062312574)