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NDC 45802-0493-98 Ammonium Lactate 12 g/100g Details
Ammonium Lactate 12 g/100g
Ammonium Lactate is a TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Padagis Israel Pharmaceuticals Ltd. The primary component is AMMONIUM LACTATE.
MedlinePlus Drug Summary
Ammonium lactate is used to treat xerosis (dry or scaly skin) and ichthyosis vulgaris (an inherited dry skin condition) in adults and children. Ammonium lactate is in a class of medications called alpha-hydroxy acids. It works by increasing skin hydration.
Related Packages: 45802-0493-98Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ammonium Lactate Topical
Product Information
| NDC | 45802-0493 |
|---|---|
| Product ID | 45802-493_5b291cbb-d47e-4aa7-ad5d-c43a05d7ba4f |
| Associated GPIs | 90650015003730 |
| GCN Sequence Number | 028191 |
| GCN Sequence Number Description | ammonium lactate CREAM (G) 12 % TOPICAL |
| HIC3 | L2A |
| HIC3 Description | EMOLLIENTS |
| GCN | 23043 |
| HICL Sequence Number | 015560 |
| HICL Sequence Number Description | AMMONIUM LACTATE |
| Brand/Generic | Generic |
| Proprietary Name | Ammonium Lactate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ammonium Lactate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 12 |
| Active Ingredient Units | g/100g |
| Substance Name | AMMONIUM LACTATE |
| Labeler Name | Padagis Israel Pharmaceuticals Ltd |
| Pharmaceutical Class | Acidifying Activity [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075774 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 45802-0493-98 (45802049398)
| NDC Package Code | 45802-493-98 |
|---|---|
| Billing NDC | 45802049398 |
| Package | 140 g in 1 TUBE (45802-493-98) |
| Marketing Start Date | 2006-08-16 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |