genrx anti-bacterial gel
Generic: alcohol
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
genrx anti-bacterial gel
Generic Name
alcohol
Labeler
puretek corporation
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 62 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
59088-299
Product ID
59088-299_23733118-0f3a-e4a8-e063-6394a90aa41e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M014
Listing Expiration
2026-12-31
Marketing Start
2020-03-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088299
Hyphenated Format
59088-299
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
genrx anti-bacterial gel (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
M014 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 62 mL/100mL
Packaging
- 118 mL in 1 BOTTLE, PUMP (59088-299-08)
- 500 mL in 1 BOTTLE, DISPENSING (59088-299-31)
- 710 mL in 1 BOTTLE, PUMP (59088-299-39)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "23733118-0f3a-e4a8-e063-6394a90aa41e", "openfda": {"upc": ["0731477342194"], "unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["a124e37e-1a44-212a-e053-2995a90a0af0"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PUMP (59088-299-08)", "package_ndc": "59088-299-08", "marketing_start_date": "20200318"}, {"sample": false, "description": "500 mL in 1 BOTTLE, DISPENSING (59088-299-31)", "package_ndc": "59088-299-31", "marketing_start_date": "20200318"}, {"sample": false, "description": "710 mL in 1 BOTTLE, PUMP (59088-299-39)", "package_ndc": "59088-299-39", "marketing_start_date": "20200318"}], "brand_name": "GenRx Anti-Bacterial Gel", "product_id": "59088-299_23733118-0f3a-e4a8-e063-6394a90aa41e", "dosage_form": "LIQUID", "product_ndc": "59088-299", "generic_name": "Alcohol", "labeler_name": "PureTek Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GenRx Anti-Bacterial Gel", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mL/100mL"}], "application_number": "M014", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200318", "listing_expiration_date": "20261231"}