curasore
Generic: pramoxine hydrochloride
Labeler: s.s.s. companyDrug Facts
Product Profile
Brand Name
curasore
Generic Name
pramoxine hydrochloride
Labeler
s.s.s. company
Dosage Form
LIQUID
Routes
Active Ingredients
pramoxine hydrochloride 1 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
12258-223
Product ID
12258-223_47e0a9b6-4f7a-b034-e063-6394a90a64ba
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2027-12-31
Marketing Start
1995-08-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
12258223
Hyphenated Format
12258-223
Supplemental Identifiers
RxCUI
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
curasore (source: ndc)
Generic Name
pramoxine hydrochloride (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100mL
Packaging
- 1 BOTTLE in 1 CARTON (12258-223-05) / 15 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47e0a9b6-4f7a-b034-e063-6394a90a64ba", "openfda": {"unii": ["88AYB867L5"], "rxcui": ["1294034", "2109512"], "spl_set_id": ["6891e5aa-e6f2-4355-8ee9-d23c9959787e"], "manufacturer_name": ["S.S.S. Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (12258-223-05) / 15 mL in 1 BOTTLE", "package_ndc": "12258-223-05", "marketing_start_date": "19950831"}], "brand_name": "Curasore", "product_id": "12258-223_47e0a9b6-4f7a-b034-e063-6394a90a64ba", "dosage_form": "LIQUID", "product_ndc": "12258-223", "generic_name": "Pramoxine Hydrochloride", "labeler_name": "S.S.S. Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Curasore", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19950831", "listing_expiration_date": "20271231"}