Itch Relief
- Product NDC
- 13709-351
- 11-digit product format
- 137090351
- Labeler code
- 13709
- Product ID
- 13709-351_44811828-c32f-17fc-e063-6294a90add48
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Itch Relief Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Neilmed Pharmaceuticals Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-26
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Itch Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
| Rxcui | 1049880 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 13709-351-01 | Itch Relief | 1 in 1 CARTON | GEL | 1 | | 1 |
| 13709-351-01 | Itch Relief | 103.5 mL in 1 TUBE | GEL | 103.5 | | 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 |
|---|
| 13709-351-01 | 13709035101 | 1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE | 1 tube | 2025-11-26 | No | No | Current |