dermacinrx zrm pak
Generic: lidocaine, dimethicone
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
dermacinrx zrm pak
Generic Name
lidocaine, dimethicone
Labeler
puretek corporation
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
59088-805
Product ID
59088-805_2baebf45-d382-1bfe-e063-6394a90aa37f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2016-05-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088805
Hyphenated Format
59088-805
Supplemental Identifiers
RxCUI
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
dermacinrx zrm pak (source: ndc)
Generic Name
lidocaine, dimethicone (source: ndc)
Resolved Composition
Strengths
- 5 %
- 5.0 %
Packaging
- 1 KIT in 1 KIT (59088-805-00) * 118 mL in 1 TUBE (59088-333-08) * 15 POUCH in 1 CARTON (59088-396-82) / .7 g in 1 POUCH
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "2baebf45-d382-1bfe-e063-6394a90aa37f", "openfda": {"rxcui": ["259090", "1745091"], "spl_set_id": ["57c4672d-37b1-4af3-a9fc-d8390016338d"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (59088-805-00) * 118 mL in 1 TUBE (59088-333-08) * 15 POUCH in 1 CARTON (59088-396-82) / .7 g in 1 POUCH", "package_ndc": "59088-805-00", "marketing_start_date": "20160512"}], "brand_name": "DermacinRx ZRM Pak", "product_id": "59088-805_2baebf45-d382-1bfe-e063-6394a90aa37f", "dosage_form": "KIT", "product_ndc": "59088-805", "generic_name": "lidocaine, dimethicone", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DermacinRx ZRM Pak", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160512", "listing_expiration_date": "20261231"}