Infant Gas Relief
Simethicone · Suspension/ Drops · Oral
Active ingredient
Active ingredient (in each 0.3 mL) Simethicone 20 mg
Purpose
Purpose Antigas
Uses
Use relieves the symptoms referred to as gas
Warnings
Warnings Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away.
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.
Directions
Directions shake well before using all dosages may be repeated as needed, after meals and at bedtime, or as directed by a physician do not exceed 12 doses per day fill enclosed dropper to recommended dosage level and dispense liquid slowly into baby’s mouth, toward inner cheek dosage can also be mixed with 1 oz. of cool water, infan formula or other suitable liquids clean dropper well after each use and replace original cap on bottle Age (years) Weight (lbs) Dose infants (under 2) under 24 0.3 mL children (over 2) 24 and over 0.6 mL
Other information
Other information store at room temperature do not freeze see bottom panel for lot number and expiration date
Inactive ingredients
Inactive ingredients carboxymethylcellulose sodium, citric acid, flavor, maltitol, microcrystalline cellulose, purified water, sodium benzoate, sodium citrate, xanthan gum. Questions or comments? 1-800-540-3765
Questions?
Questions or comments? 1-800-540-3765
Label text from the FDA structured product label by AMERISOURCEBERGEN DRUG CORPORATION (revised Jul 18, 2023). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Dimethicone in 1 product
Infant Gas Relief NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 46122-547 | Dimethicone 20 mg/.3mL Suspension/ Drops | AMERISOURCEBERGEN DRUG CORPORATION | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Infant Gas Relief used for?
Use relieves the symptoms referred to as gas
Who makes Infant Gas Relief?
Infant Gas Relief is listed by 1 labeler in the FDA NDC directory, including AMERISOURCEBERGEN DRUG CORPORATION.