OTC - PURPOSE SECTION
Silagen
- Manufacturer
- NewMedical Technology Inc.
- Effective date
- 2023-06-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 9
- Source
- full-release
- Hydrated at
- 2026-05-31 23:55:11
Label at a glance#
ProductSilagen
Active ingredientZINC OXIDE
Label structure6 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
WARNINGS SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - ACTIVE INGREDIENT SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69291-6215-1 | Silagen | 1 in 1 CARTON | GEL | 1 | 9 | |
| 69291-6215-2 | Silagen | 15 g in 1 BOTTLE, PUMP | GEL | 15 | 9 | |
| 69291-6230-1 | Silagen | 1 in 1 CARTON | GEL | 1 | 9 | |
| 69291-6230-2 | Silagen | 30 g in 1 BOTTLE, PUMP | GEL | 30 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69291-6215 | SILAGEN (ZINC OXIDE, SUNSCREEN) GEL [NEWMEDICAL TECHNOLOGY INC.] | 9 | Legacy NDC, 2 package rows | 20230609_486c44cd-47b3-537d-e054-00144ff8d46c.zip |
| 69291-6230 | SILAGEN (ZINC OXIDE, SUNSCREEN) GEL [NEWMEDICAL TECHNOLOGY INC.] | 9 | Legacy NDC, 2 package rows | 20230609_486c44cd-47b3-537d-e054-00144ff8d46c.zip |
Products#
Every source-derived product name is available through these pages.
- Silagen
- Zinc Oxide, Sunscreen
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)
- ALKYL (C12-15) BENZOATE
- POLYHYDROXYSTEARIC ACID (2300 MW)
- ZINC OXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69291-6215 | 69291-6215-2, 69291-6215-1 |
| 69291-6230 | 69291-6230-2, 69291-6230-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| fda3bd7d-76cd-ca9b-e053-6394a90a4ec9 | 486c44cd-47b3-537d-e054-00144ff8d46c | 2023-06-08 | Warnings | fda3bd7d-76cd-ca9b-e053-6394a90a4ec9 486c44cd-47b3-537d-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.