Itch Relief Gel
- Product NDC
- 82645-901
- 11-digit product format
- 826450901
- Labeler code
- 82645
- Product ID
- 82645-901_0d1cd578-e127-6e8e-e063-6294a90a5060
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Itch Relief Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Pharma Nobis, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-20
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 2 mg/100mL
- 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 Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 2 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82645-901-94 | Itch Relief Gel | 118 mL in 1 CONTAINER | GEL | 118 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82645-901 | ITCH RELIEF GEL GEL [PHARMA NOBIS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231223_e42f484d-a641-3489-e053-2a95a90a4254.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82645-901-94 | 82645090194 | 118 mL in 1 CONTAINER (82645-901-94) | 118 ml | 2018-12-20 | 0000-00-00 | No | No | Current |