itch relief

Generic: itch relief gel

Labeler: neilmed pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name itch relief
Generic Name itch relief gel
Labeler neilmed pharmaceuticals inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diphenhydramine hydrochloride 20 mg/mL

Manufacturer
Neilmed Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 13709-351
Product ID 13709-351_44811828-c32f-17fc-e063-6294a90add48
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-11-26

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13709351
Hyphenated Format 13709-351

Supplemental Identifiers

RxCUI
1049880
UNII
TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name itch relief (source: ndc)
Generic Name itch relief gel (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE
source: ndc

Packages (1)

13709-351-01 1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE

Ingredients (1)

diphenhydramine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Itch Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "44811828-c32f-17fc-e063-6294a90add48", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049880"], "spl_set_id": ["44811828-c32e-17fc-e063-6294a90add48"], "manufacturer_name": ["Neilmed Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (13709-351-01)  / 103.5 mL in 1 TUBE", "package_ndc": "13709-351-01", "marketing_start_date": "20251126"}], "brand_name": "Itch Relief", "product_id": "13709-351_44811828-c32f-17fc-e063-6294a90add48", "dosage_form": "GEL", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "13709-351", "generic_name": "Itch Relief Gel", "labeler_name": "Neilmed Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251126", "listing_expiration_date": "20261231"}