ethyl rubbing alcohol 70 percent
Generic: ethyl alcohol
Labeler: pharma nobis, llcDrug Facts
Product Profile
Brand Name
ethyl rubbing alcohol 70 percent
Generic Name
ethyl alcohol
Labeler
pharma nobis, llc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 700 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
82645-926
Product ID
82645-926_0d6cc629-bac2-1229-e063-6294a90a2610
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2016-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82645926
Hyphenated Format
82645-926
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
ethyl rubbing alcohol 70 percent (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 700 mg/mL
Packaging
- 473 mL in 1 BOTTLE (82645-926-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0d6cc629-bac2-1229-e063-6294a90a2610", "openfda": {"upc": ["0087701427244"], "unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["e42fccc2-1b50-e7f3-e053-2a95a90aef39"], "manufacturer_name": ["Pharma Nobis, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (82645-926-16)", "package_ndc": "82645-926-16", "marketing_start_date": "20160101"}], "brand_name": "Ethyl Rubbing Alcohol 70 Percent", "product_id": "82645-926_0d6cc629-bac2-1229-e063-6294a90a2610", "dosage_form": "LIQUID", "product_ndc": "82645-926", "generic_name": "ethyl alcohol", "labeler_name": "Pharma Nobis, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ethyl Rubbing Alcohol 70 Percent", "active_ingredients": [{"name": "ALCOHOL", "strength": "700 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}