natureplex psoriasis
Generic: salicylic acid
Labeler: natureplex, llcDrug Facts
Product Profile
Brand Name
natureplex psoriasis
Generic Name
salicylic acid
Labeler
natureplex, llc
Dosage Form
CREAM
Routes
Active Ingredients
salicylic acid 20 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
67234-073
Product ID
67234-073_31269712-42a5-44bd-8f6f-196f934d75c4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2027-12-31
Marketing Start
2019-07-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67234073
Hyphenated Format
67234-073
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
natureplex psoriasis (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 TUBE in 1 CARTON (67234-073-01) / 28 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "31269712-42a5-44bd-8f6f-196f934d75c4", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["317152"], "spl_set_id": ["1efa3e8d-f80b-44f4-a233-187e3329dd8f"], "manufacturer_name": ["Natureplex, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (67234-073-01) / 28 g in 1 TUBE", "package_ndc": "67234-073-01", "marketing_start_date": "20190724"}], "brand_name": "NATUREPLEX PSORIASIS", "product_id": "67234-073_31269712-42a5-44bd-8f6f-196f934d75c4", "dosage_form": "CREAM", "product_ndc": "67234-073", "generic_name": "SALICYLIC ACID", "labeler_name": "Natureplex, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NATUREPLEX PSORIASIS", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/g"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190724", "listing_expiration_date": "20271231"}