NDC 81033-014-30 - Milk of Magnesia
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 81033-014
- Requested NDC
- 81033-014-30
- Package NDCs from labels
- 81033-014-30, 81033-014-52
- Manufacturer
- Kesin Pharma Corporation
- Effective date
- 2025-09-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Milk of Magnesia - Kesin Pharma Corporation | Kesin Pharma Corporation | 2025-09-23 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-014-30 | Milk of Magnesia | 30 mL in 1 CUP, UNIT-DOSE | SUSPENSION | 30 | 1 | |
| 81033-014-52 | Milk of Magnesia | 100 in 1 CASE | SUSPENSION | 100 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-014-30 | ML - Milliliter | 81033-014 | d8616778-365a-4d08-a850-8d28d62c0ff6 | 1 | 2025-11-13 |
| 81033-014-52 | ML - Milliliter | 81033-014 | 3ebe1f74-0115-4a62-9727-4e7b74514298 | 1 | 2025-11-13 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Bambusa Pulsatilla | BAMBUSA PULSATILLA | Uriel Pharmacy Inc. | 0776c3be-088d-422c-9c12-08fcaae823e1 | 2025-11-26 | Warnings | ETJ7Z6XBU4 |
| Splash Pure PF | PROPYLENE GLYCOL | LABORATORIOS SOPHIA, S.A. DE C.V. | 40ad7ae5-1f2a-e3b1-e063-6294a90a6f84 | 2025-11-26 | Warnings | 6DC9Q167V3 |
| Walgreen Fiber Lax | CALCIUM POLYCARBOPHIL | WALGREENS CO. | 9cbe1798-e0dc-4a90-bd91-8696fc59b2a6 | 2025-11-25 | Warnings | M007 |
| Walgreens Fiber Therapy | METHYLCELLULOSE | WALGREENS CO. | 6401a2c3-5869-4898-81db-3cd7151ca69a | 2025-11-25 | Warnings | M007 |
| Walgreens Childrens Saline Laxative | MAGNESIUM HYDROXIDE | WALGREEN CO. | 3813ed22-cf68-4c16-9b61-c39828120079 | 2025-11-25 | Warnings | NBZ3QY004S |
| Walgreens Senna Laxative | SENNOSIDES | WALGREENS CO. | a95bd796-d85e-4599-bbb1-2170088fa937 | 2025-11-25 | Warnings | M007 |
| Walgreens Stool Softener Fruit Punch | DOCUSATE SODIUM | WALGREENS CO. | 8428c81d-227a-4b0f-9a47-71d6a6983842 | 2025-11-25 | Warnings | M007 |
| Thyroid-Adrenal | ADRENALINUM, THYROIDINUM, ALOE, CALC. CARB., CHELIDONIUM MAJUS, CONIUM, GRAPHITES, IODIUM, LACHESIS, LYCOPODIUM, LYCOPUS VIRGINICUS, PHYTOLACCA, RHUS TOXICODENDRON, SILICEA, SPONGIA, ECHINACEA | Newton Laboratories, Inc. | b597504a-c667-225c-e053-2a95a90ac704 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| DOCTRUST ONE S Tooth | SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE | DONG IL PHARMS CO.,LTD | 4476923a-48f1-9f72-e063-6394a90a0708 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 44768dd1-b132-c33b-e063-6294a90accd4 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| Stool Softener Laxative | DOCUSATE SODIUM | The Kroger Co. | 9019ae9e-da3e-4ed1-b83e-d9a6375e9c30 | 2025-11-25 | Warnings | M007 |
| Gout Pain Management | ARNICA MONTANA, URTICA URENS, SILICON DIOXIDE, AND THUJA OCCIDENTALIS LEAF | Forces of Nature | 9276fe9c-d9a2-4cef-986c-5d7d39f2d6a1 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| Stool Softener Laxative | DOCUSATE SODIUM | Family Dollar (FAMILY WELLNESS) | d61ba4ef-5b03-4d29-b1fd-81591f0c8a2c | 2025-11-25 | Warnings | M007 |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| Eyewash Station Additive Concentrate | CHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOL | Niagara Pharmaceuticals Inc. | 362a6b6d-862d-4322-87a8-5b3a07fbe174 | 2025-11-24 | Warnings | 6DC9Q167V3 |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.