Itch Relief
- Product NDC
- 61010-8300
- 11-digit product format
- 610108300
- Labeler code
- 61010
- Product ID
- 61010-8300_109674e0-ef83-5844-e063-6394a90ae6b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine hydrochloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Safetec of America, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-05-02
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 20.3 g/L
- 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 | 20.3 g/L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
| Rxcui | 1050080 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61010-8300-1 | Itch Relief | 0.0591 L in 1 BOTTLE, SPRAY | LIQUID | 0.0591 | | 3 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| diphenhydramine hydrochloride | ACTIVE INGREDIENT | TC2D6JAD40 | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| diphenhydramine | ACTIVE MOIETY | 8GTS82S83M | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| C12-15 PARETH-9 | INACTIVE INGREDIENT | H3ZIY6WP1R | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| diazolidinyl urea | INACTIVE INGREDIENT | H5RIZ3MPW4 | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| edetate disodium | INACTIVE INGREDIENT | 7FLD91C86K | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| trolamine | INACTIVE INGREDIENT | 9O3K93S3TK | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61010-8300 | ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [SAFETEC OF AMERICA, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240214_4f4c801b-d894-4fa3-b024-6ca41a5f2a95.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61010-8300-1 | 61010830001 | .0591 L in 1 BOTTLE, SPRAY (61010-8300-1) | 2013-05-02 | 0000-00-00 | No | No | Current |