extra strength itch stopping

Generic: itch stopping cream

Labeler: universal distribution centre llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength itch stopping
Generic Name itch stopping cream
Labeler universal distribution centre llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

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

Manufacturer
Universal Distribution Centre LLC

Identifiers & Regulatory

Product NDC 52000-071
Product ID 52000-071_1853be3d-62de-dc6b-e063-6394a90aad99
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2021-01-21

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 52000071
Hyphenated Format 52000-071

Supplemental Identifiers

RxCUI
1087026
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 stopping (source: ndc)
Generic Name itch stopping cream (source: ndc)
Application Number M016 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (52000-071-04) / 35.4 g in 1 TUBE (52000-071-03)
source: ndc

Packages (1)

52000-071-04 1 TUBE in 1 CARTON (52000-071-04) / 35.4 g in 1 TUBE (52000-071-03)

Ingredients (2)

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

Linked Drug Pages (1)

Extra Strength Itch Stopping ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1853be3d-62de-dc6b-e063-6394a90aad99", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1087026"], "spl_set_id": ["b9a42aa3-1903-76f0-e053-2a95a90a51d1"], "manufacturer_name": ["Universal Distribution Centre LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (52000-071-04)  / 35.4 g in 1 TUBE (52000-071-03)", "package_ndc": "52000-071-04", "marketing_start_date": "20210121"}], "brand_name": "Extra Strength Itch Stopping", "product_id": "52000-071_1853be3d-62de-dc6b-e063-6394a90aad99", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "52000-071", "generic_name": "Itch Stopping Cream", "labeler_name": "Universal Distribution Centre LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength", "brand_name_suffix": "Itch Stopping", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210121", "listing_expiration_date": "20261231"}