Aluminum Hydroxide
- Product NDC
- 17856-0091
- 11-digit product format
- 178560091
- Labeler code
- 17856
- Product ID
- 17856-0091_4602216a-bb8c-af52-e063-6294a90a380e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- M
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2005-02-01
- Substance
- ALUMINUM HYDROXIDE
- Active strength
- 320 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aluminum Hydroxide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM HYDROXIDE | 320 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QB0T2IUN0 |
| Rxcui | 308078 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0091-3 | Aluminum Hydroxide | 30 mL in 1 CUP | LIQUID | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0091 | ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) LIQUID [ATLANTIC BIOLOGICALS CORP.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250514_60a54d4e-89c2-4329-86bf-a288527f37b5.zip |
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 |
|---|
| 17856-0091-3 | 17856009103 | 30 mL in 1 CUP (17856-0091-3) | 30 ml | 2024-04-16 | 0000-00-00 | No | No | Current |