pramoxine itch relief
Generic: pramoxine hcl 1%
Labeler: cvsDrug Facts
Product Profile
Brand Name
pramoxine itch relief
Generic Name
pramoxine hcl 1%
Labeler
cvs
Dosage Form
CREAM
Routes
Active Ingredients
pramoxine hydrochloride 1 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
51316-141
Product ID
51316-141_28f13725-48d9-8774-e063-6394a90a6704
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2023-04-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316141
Hyphenated Format
51316-141
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
pramoxine itch relief (source: ndc)
Generic Name
pramoxine hcl 1% (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100g
Packaging
- 340 g in 1 JAR (51316-141-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "28f13725-48d9-8774-e063-6394a90a6704", "openfda": {"upc": ["0050428277805"], "unii": ["88AYB867L5"], "rxcui": ["1052684"], "spl_set_id": ["e947694c-c122-0291-e053-2995a90ac39a"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "340 g in 1 JAR (51316-141-12)", "package_ndc": "51316-141-12", "marketing_start_date": "20230425"}], "brand_name": "Pramoxine Itch relief", "product_id": "51316-141_28f13725-48d9-8774-e063-6394a90a6704", "dosage_form": "CREAM", "product_ndc": "51316-141", "generic_name": "Pramoxine HCl 1%", "labeler_name": "CVS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pramoxine Itch relief", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230425", "listing_expiration_date": "20261231"}