SANAR NATURALS CHILDRENS PAIN RELIEVER- acetaminophen liquid

Sanar Naturals Childrens Pain Reliever by

Drug Labeling and Warnings

Sanar Naturals Childrens Pain Reliever by is a Otc medication manufactured, distributed, or labeled by Sanvall Enterprises, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Acetaminophen 160mg

Purpose

Pain reliever/fever reducer

Uses

• reduces fever
• relieves minor aches and pains due to:
• the common cold
• flu
• headache
• sore throat
• toothache

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.

Ask a Doctor

your child has liver disease.

Ask a doctor or pharmacist before use

your child is taking the blood thinning drug warfarin.

When using this product do not exceed recommended dose

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

Keep out of reach of children

in case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222- 1222)

Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

This product does not contain directions or complete warnings for adult use. Do not give more than directed (see overdose warning). Shake well before using. ml=milliliter. Find right dose on chart below. If possible, use weight to dose; otherwise, use age.

Remove the child protective cap and squeeze your child's dose into the dosing cup. Repeat dose every 4 hours while symptoms last, do not give more than 5 times in 24 hours.

Weight (lb)	Age (yr)	Dose (ml)*
under 24	under 2 years	ask a doctor
24-35	2-3 years	5 ml
36-47	4-5 years	7.5 ml
48-59	6-8 years	10 ml
60-71	9-10 years	12.5 ml
72-95	11 years	15 ml

*or as directed by a doctor

Attention use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.

Inactive Ingredients

Flavor, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium carboxymethylcellulose and sucralose.

Other Information

www.sanarnaturals.com

Sanar Naturals Children's Pain + Fever

INGREDIENTS AND APPEARANCE

SANAR NATURALS CHILDRENS PAIN RELIEVER 
acetaminophen liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73386-324
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
PROPYLPARABEN (UNII: Z8IX2SC1OH)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color		Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73386-324-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	02/05/2024

Labeler - Sanvall Enterprises, Inc. (966905507)

Registrant - Sanvall Enterprises, Inc. (966905507)