DailyMed label
Oxaltem
DailyMed label · Nucleic Products, LLC · version 4
Key facts
| Product | Oxaltem |
|---|---|
| Labeler | Nucleic Products, LLC |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | BERBERIS VULGARIS ROOT BARK, CALCIUM FLUORIDE, CALCIUM SILICATE, CHIMAPHILA UMBELLATA WHOLE, OXALIC ACID, PARATHYROID HORMONE, PYRIDOXINE HYDROCHLORIDE, SANGUINARIA CANADENSIS WHOLE, TRIBASIC CALCIUM PHOSPHATE, URIC ACID |
| Active ingredient UNIIs | 1TH8Q20J0U, 268B43MJ25, 68Y4CF58BV, 91D9GV0Z28, 9E7R5L6H31, B3XJA0OV6T, N19A0T0E5J, O3B55K4YKI, S4255P4G5M, WCK21A9W9J |
| Route | ORAL |
| NDC package codes | 75053-0009-1 |
| Effective date | May 13, 2024 |
| Set ID | ab35fadf-5213-486b-b313-e676420efff7 |
At a glance
- 1–9 NDC package codes
- 10–99 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: