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NDC 00363-0193-13 Sodium Chloride 50 mg/mL Details
Sodium Chloride 50 mg/mL
Sodium Chloride is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 00363-0193 |
|---|---|
| Product ID | 0363-0193_faeb782d-9560-7324-e053-6394a90a22bf |
| Associated GPIs | 43998903350920 |
| GCN Sequence Number | 053178 |
| GCN Sequence Number Description | DM/acetaminophen/doxylamine LIQUID 30-12.5/30 ORAL |
| HIC3 | B4G |
| HIC3 Description | NON-OPIOID ANTITUS-1ST GEN ANTIHIST-ANALGESIC COMB |
| GCN | 20556 |
| HICL Sequence Number | 025663 |
| HICL Sequence Number Description | DEXTROMETHORPHAN HBR/ACETAMINOPHEN/DOXYLAMINE |
| Brand/Generic | Generic |
| Proprietary Name | Sodium Chloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sodium Chloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | SODIUM CHLORIDE |
| Labeler Name | Walgreen Company |
| Pharmaceutical Class | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part349 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00363-0193-13 (00363019313)
| NDC Package Code | 0363-0193-13 |
|---|---|
| Billing NDC | 00363019313 |
| Package | 1 BOTTLE, DROPPER in 1 BOX (0363-0193-13) / 15 mL in 1 BOTTLE, DROPPER |
| Marketing Start Date | 2019-04-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |