CVS Itch Relief
- Product NDC
- 51316-624
- 11-digit product format
- 513160624
- Labeler code
- 51316
- Product ID
- 51316-624_46921bea-fcbf-94d6-e063-6394a90a726b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pramoxine Hydrochloride, Zinc Acetate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- CVS Pharmacy
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-22
- Substance
- PRAMOXINE HYDROCHLORIDE; ZINC ACETATE DIHYDRATE
- Active strength
- 10; 1 mg/g; mg/g
- 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
- CVS Itch Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAMOXINE HYDROCHLORIDE | 10 mg/g |
| ZINC ACETATE DIHYDRATE | 1 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 88AYB867L5, FM5526K07A |
| Rxcui | 1294033 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-624-03 | CVS Itch Relief | 85 g in 1 CAN | SPRAY | 85 | | 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 |
|---|
| 51316-624-03 | 51316062403 | 85 g in 1 CAN (51316-624-03) | 85 g | 2025-12-22 | No | No | Current |