Aluminum Hydroxide
- Product NDC
- 24451-091
- 11-digit product format
- 244510091
- Labeler code
- 24451
- Product ID
- 24451-091_18de8a4b-df09-498a-ab6b-df914a59e48a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Hydroxide
- Dosage form
- GEL
- Route
- ORAL
- Labeler
- LLC Federal Solutions
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-08-12
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM HYDROXIDE
- Active strength
- 320 mg/5mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24451-091-30 | Aluminum Hydroxide | 30 mL in 1 CUP, UNIT-DOSE | GEL | 30 | | 1 |
| 24451-091-30 | Aluminum Hydroxide | 100 in 1 BOX | GEL | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24451-091 | ALUMINUM HYDROXIDE GEL [LLC FEDERAL SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20130816_af9b799f-69c5-401c-9c43-a97b23384cc2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 24451-091-30 | 24451009130 | 30 mL in 1 CUP, UNIT-DOSE | 30 ml | Historical |