extra strength itch relief

Generic: diphenhydramine hcl and zinc acetate

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength itch relief
Generic Name diphenhydramine hcl and zinc acetate
Labeler chain drug marketing association inc
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

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

Manufacturer
Chain Drug Marketing Association Inc

Identifiers & Regulatory

Product NDC 83324-302
Product ID 83324-302_42f3fe19-b76d-2a12-e063-6394a90afd7f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2024-06-06

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 83324302
Hyphenated Format 83324-302

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 extra strength itch relief (source: ndc)
Generic Name diphenhydramine hcl and zinc acetate (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
  • 1 mg/g
source: ndc
Packaging
  • 76 g in 1 CAN (83324-302-27)
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "42f3fe19-b76d-2a12-e063-6394a90afd7f", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1053138"], "spl_set_id": ["1a2997bc-7741-e658-e063-6394a90af6fd"], "manufacturer_name": ["Chain Drug Marketing Association Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "76 g in 1 CAN (83324-302-27)", "package_ndc": "83324-302-27", "marketing_start_date": "20240606"}], "brand_name": "Extra Strength Itch Relief", "product_id": "83324-302_42f3fe19-b76d-2a12-e063-6394a90afd7f", "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": "83324-302", "generic_name": "Diphenhydramine HCl and Zinc Acetate", "labeler_name": "Chain Drug Marketing Association Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240606", "listing_expiration_date": "20261231"}