Home NDC 49035-709 Infants Gas Relief Drops
Product NDC 49035-709
11-digit product format 490350709
Labeler code 49035
Product ID 49035-709_42223d4a-ac52-c3c5-e063-6394a90a3723
Type HUMAN OTC DRUG
Nonproprietary name Simethicone
Dosage form EMULSION
Route ORAL
Labeler Wal-Mart Stores,Inc.,
Application M002
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-10-16
Substance DIMETHICONE, UNSPECIFIED
Active strength 20 mg/.3mL
Pharmacologic classes Skin Barrier Activity [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Infants Gas Relief Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE, UNSPECIFIED 20 mg/.3mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198857 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49035-709-01 Infants Gas Relief Drops 1 in 1 CARTON EMULSION 1 12 49035-709-01 Infants Gas Relief Drops 30 mL in 1 BOTTLE EMULSION 30 12 49035-709-30 Infants Gas Relief Drops 30 mL in 1 BOTTLE EMULSION 30 12 49035-709-30 Infants Gas Relief Drops 1 in 1 CARTON EMULSION 1 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-709 INFANTS GAS RELIEF DROPS (SIMETHICONE) EMULSION [WAL-MART STORES,INC.,] 11 Current NDC, Legacy NDC, 4 package rows 20241116_966f0506-c2d2-4d3c-bd2d-c5a6b1e0a157.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 13 · 255 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49035-709-01 49035070901 1 BOTTLE in 1 CARTON (49035-709-01) / 30 mL in 1 BOTTLE 1 bottle 2017-10-16 0000-00-00 No No Current 49035-709-30 49035070930 1 BOTTLE in 1 CARTON (49035-709-30) / 30 mL in 1 BOTTLE 1 bottle 2019-10-22 0000-00-00 No No Current