Label: MAX RELIEF JUNIOR- acetaminophen liquid
- NDC Code(s): 71399-0021-4, 71399-0021-6, 71399-0021-8
- Packager: Akron Pharma Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 17, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
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.
Soar throat warning: if sore throat is severe, persists or 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.
Ask a doctor before use if your child has liver disease.
Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin.
When using this product: Do not exceed recommended dose (see overdose warning)
Stop use and ask a doctor if
- pain gets worse or lasts more than 5 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.
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- SPL UNCLASSIFIED SECTION
-
DOSAGE & ADMINISTRATION
Directions
- this product does not contain direction or complete warnings for adult use
- Shake well before using
- ml = milliliter
- find right dose on chart below
- if possible, use weight to dose; otherwise use age
- use only the enclosed dosing cup designed for use with this product. Do not use any other dosing device.
- if needed, repeat dose every 4 hourswhile symptoms last
- do not give more than 5 times in 24 hours
- do not give more than 5 days unless directed by doctor.
Weight (lbs.) Age (yrs.) Dose (tsp or mL) under 24 under 2 ask a doctor 24 to 35 2 to 3 1 tsp or 5 mL 36 to 47 4 to 5 1 1/2 tsp or 7.5 mL 48 to 59 6 to 8 2 tsp or 10 mL 60 to 71 9 to 10 2 1/2 tsp or 12.5 mL 72 to 95 11 3 tsp or 15 mL Other Information store at room temperature 15o-30oC (59o-86oF). Protect from Freezing. Protect from light.
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MAX RELIEF JUNIOR
acetaminophen liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71399-0021 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 160 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color Score Shape Size Flavor BUBBLE GUM Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71399-0021-4 1 in 1 PACKAGE 05/14/2023 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:71399-0021-8 1 in 1 PACKAGE 05/14/2023 2 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:71399-0021-6 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/14/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 05/14/2023 Labeler - Akron Pharma Inc. (067878881)