itch relief

Generic: diphenhydramine hcl, zinc acetate

Labeler: cardinal health, 110 dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name itch relief
Generic Name diphenhydramine hcl, zinc acetate
Labeler cardinal health, 110 dba leader
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

diphenhydramine hydrochloride 20 mg/mL, zinc acetate 1 mg/mL

Manufacturer
Cardinal Health, 110 dba Leader

Identifiers & Regulatory

Product NDC 70000-0023
Product ID 70000-0023_498e72fe-ddb9-18ce-e063-6394a90a8aee
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2011-08-02

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000023
Hyphenated Format 70000-0023

Supplemental Identifiers

RxCUI
1053138
UNII
TC2D6JAD40 FM5526K07A

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 diphenhydramine hcl, zinc acetate (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
  • 1 mg/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, SPRAY (70000-0023-1)
source: ndc

Packages (1)

Ingredients (2)

diphenhydramine hydrochloride (20 mg/mL) zinc acetate (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "498e72fe-ddb9-18ce-e063-6394a90a8aee", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1053138"], "spl_set_id": ["3ed7b8a1-012f-459d-878c-813b93d4673c"], "manufacturer_name": ["Cardinal Health, 110 dba Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, SPRAY (70000-0023-1)", "package_ndc": "70000-0023-1", "marketing_start_date": "20110802"}], "brand_name": "Itch Relief", "product_id": "70000-0023_498e72fe-ddb9-18ce-e063-6394a90a8aee", "dosage_form": "SPRAY", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70000-0023", "generic_name": "Diphenhydramine HCl, Zinc Acetate", "labeler_name": "Cardinal Health, 110 dba Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}, {"name": "ZINC ACETATE", "strength": "1 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110802", "listing_expiration_date": "20271231"}