ZEUS
- Product NDC
- 84697-001
- 11-digit product format
- 846970001
- Labeler code
- 84697
- Product ID
- 84697-001_436d9732-c5cf-9e81-e063-6394a90a902c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NEWPORT APOTHECARY, INC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-26
- Substance
- ZINC OXIDE
- Active strength
- 22.3 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ZEUS
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 22.3 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84697-001-01 | ZEUS | 50 mL in 1 BOTTLE | CREAM | 50 | | 3 |
| 84697-001-01 | ZEUS | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84697-001 | ZEUS (ZINC OXIDE) CREAM [NEWPORT APOTHECARY, INC] | 1 | Current NDC, 2 package rows | 20241004_5354c383-08f0-4b89-b36a-96a35f47be3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84697-001-01 | 84697000101 | 1 BOTTLE in 1 CARTON (84697-001-01) / 50 mL in 1 BOTTLE | 1 bottle | 2024-09-26 | No | No | Historical |