cvs anti-itch
Generic: pramoxine hcl
Labeler: cvsDrug Facts
Product Profile
Brand Name
cvs anti-itch
Generic Name
pramoxine hcl
Labeler
cvs
Dosage Form
LOTION
Routes
Active Ingredients
pramoxine hydrochloride 1 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
69842-263
Product ID
69842-263_43fa5b19-a526-4b4a-e063-6294a90a2cda
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2016-04-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842263
Hyphenated Format
69842-263
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
cvs anti-itch (source: ndc)
Generic Name
pramoxine hcl (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100g
Packaging
- 212 g in 1 BOTTLE, PUMP (69842-263-75)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43fa5b19-a526-4b4a-e063-6294a90a2cda", "openfda": {"upc": ["0050428305881"], "unii": ["88AYB867L5"], "rxcui": ["1246075"], "spl_set_id": ["87fc476a-5b12-7383-e053-2995a90a530b"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "212 g in 1 BOTTLE, PUMP (69842-263-75)", "package_ndc": "69842-263-75", "marketing_start_date": "20160414"}], "brand_name": "CVS Anti-Itch", "product_id": "69842-263_43fa5b19-a526-4b4a-e063-6294a90a2cda", "dosage_form": "LOTION", "product_ndc": "69842-263", "generic_name": "Pramoxine HCL", "labeler_name": "CVS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Anti-Itch", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160414", "listing_expiration_date": "20261231"}