Label: PAIN AND FEVER CHILDRENS- acetaminophen tablet, chewable
- NDC Code(s): 49035-777-08, 49035-777-39
- Packager: Wal-Mart Stores Inc
- 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.
Drug Label Information
Updated February 16, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each chewable tablet)
- Purpose
- Uses
-
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if your child takes
- more than 5 doses in 24 hours, which is the maximum daily amount
- with other drugs containing acetaminophen
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.
Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
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 your child is allergic to acetaminophen or any of the inactive ingredients in this product
-
Directions
- this product does not contain directions or complete warnings for adult use
- do not give more than directed
- find the right dose on chart below. If possible, use weight to dose; otherwise, use age.
- chew or crush tablets completely before swallowing; do not swallow tablets whole
- repeat dose every 4 hours while symptoms last
- do not give more than 5 times in 24 hours
- do not give for more than 5 days unless directed by a doctor
Weight (lb) Age (yr) Dose (chewable tablets)* Under 24 Under 2 Ask a doctor 24-35 2-3 1 tablet 36-47 4-5 1 1/2 tablets 48-59 6-8 2 tablets 60-71 9-10 2 1/2 tablets 72-95 11 3 tablets *or as directed by a doctor
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
equate™
NDC 49035-777-08
Compare to
Children's
Tylenol® active
ingredient†children's
PAIN & FEVERAcetaminophen 160 mg
Chewable Tablets■ Pain Reliever / Fever Reducer
2-11 YEARS
■ Aspirin Free
■ Ibuprofen FreeBubblegum Flavor
24 Chewable Tablets
Actual Size
Chew or crush
tablets completely
before swallowing.TAMPER EVIDENT: DO NOT
USE IF PACKAGE IS OPENED
OR IF BLISTER UNIT IS
TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERINGSatisfaction guaranteed – Or we’ll
replace it or give you your money
back. For questions or comments
please call 1-888-287-1915.DISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 72716†This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of
the registered trademark Children’s Tylenol®.
50844 REV0522D45008Equate 44-450
-
INGREDIENTS AND APPEARANCE
PAIN AND FEVER CHILDRENS
acetaminophen tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-777 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 160 mg Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CROSPOVIDONE (UNII: 2S7830E561) D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX) D&C RED NO. 30 (UNII: 2S42T2808B) DEXTROSE MONOHYDRATE (UNII: LX22YL083G) ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B) MAGNESIUM STEARATE (UNII: 70097M6I30) MANNITOL (UNII: 3OWL53L36A) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) STEARIC ACID (UNII: 4ELV7Z65AP) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color pink Score 2 pieces Shape ROUND Size 16mm Flavor BUBBLE GUM Imprint Code 44;450 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-777-39 6 in 1 BLISTER PACK; Type 0: Not a Combination Product 02/25/2005 2 NDC:49035-777-08 4 in 1 CARTON 02/25/2005 2 6 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 02/25/2005 Labeler - Wal-Mart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(49035-777) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(49035-777) , pack(49035-777) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(49035-777) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(49035-777)