DailyMed label
Gelusil
DailyMed label · WellSpring Pharmaceutical Corporation · version 26
Key facts
| Product | Gelusil |
|---|---|
| Labeler | WellSpring Pharmaceutical Corporation |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | ALUMINUM HYDROXIDE, DIMETHICONE, UNSPECIFIED, MAGNESIUM HYDROXIDE, SILICON DIOXIDE |
| Active ingredient UNIIs | 5QB0T2IUN0, 92RU3N3Y1O, ETJ7Z6XBU4, NBZ3QY004S |
| Application number | M001 |
| Route | ORAL |
| NDC package codes | 65197-300-10, 65197-300-11 |
| Effective date | Nov 20, 2025 |
| Set ID | 92fbeec1-1562-40f3-9734-41f133d494f9 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- None Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: