NDC 45765-5132 - BM Maximum Diaper Rash
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
- 45765-5132
- Package NDCs from labels
- 45765-5132-0
- Manufacturer
- Naterra International INC.
- Effective date
- 2012-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BM Maximum Diaper Rash | Naterra International INC. | 2012-08-01 | COSMETIC |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Zinc Oxide | ACTIVE INGREDIENT | SOI2LOH54Z | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| Zinc Oxide | ACTIVE MOIETY | SOI2LOH54Z | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| .ALPHA.-TOCOPHEROL ACETATE | INACTIVE INGREDIENT | 9E8X80D2L0 | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| ISOPROPYL PALMITATE | INACTIVE INGREDIENT | 8CRQ2TH63M | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| LANOLIN | INACTIVE INGREDIENT | 7EV65EAW6H | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| Petrolatum | INACTIVE INGREDIENT | 4T6H12BN9U | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| SAFFLOWER OIL | INACTIVE INGREDIENT | 65UEH262IS | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | BM MAXIMUM DIAPER RASH (ZINC OXIDE) CREAM [NATERRA INTERNATIONAL INC.] | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.