Zilactin
- Product NDC
- 42829-468
- 11-digit product format
- 428290468
- Labeler code
- 42829
- Product ID
- 42829-468_42ef8c05-236d-12e9-e063-6394a90ae7d1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzyl alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ASCENT CONSUMER PRODUCTS, INC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-06
- Substance
- BENZYL ALCOHOL
- Active strength
- .1 g/g
- Pharmacologic classes
- Pediculicide [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zilactin
- Brand name suffix
- Early Relief Cold Sore
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZYL ALCOHOL | .1 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LKG8494WBH |
| Rxcui | 581456, 866357 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42829-468-02 | ZilactinEarly Relief Cold Sore | 7 g in 1 TUBE | GEL | 7 | | 1 |
| 42829-468-02 | ZilactinEarly Relief Cold Sore | 1 in 1 CARTON | GEL | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 42829-468-02 | 42829046802 | 1 TUBE in 1 CARTON (42829-468-02) / 7 g in 1 TUBE | 1 tube | 2025-11-06 | No | No | Current |