70% rubbing
Generic: isopropyl alcohol
Labeler: vi-jon, llcDrug Facts
Product Profile
Brand Name
70% rubbing
Generic Name
isopropyl alcohol
Labeler
vi-jon, llc
Dosage Form
LIQUID
Routes
Active Ingredients
isopropyl alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0869-0845
Product ID
0869-0845_38e372b4-1965-e6ac-e063-6294a90af1c9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
1989-07-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
08690845
Hyphenated Format
0869-0845
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
70% rubbing (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (0869-0845-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38e372b4-1965-e6ac-e063-6294a90af1c9", "openfda": {"unii": ["ND2M416302"], "rxcui": ["808520"], "spl_set_id": ["238029ed-e36d-4612-94d5-8cf96d60d115"], "manufacturer_name": ["Vi-Jon, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0869-0845-43)", "package_ndc": "0869-0845-43", "marketing_start_date": "19890715"}], "brand_name": "70% Rubbing", "product_id": "0869-0845_38e372b4-1965-e6ac-e063-6294a90af1c9", "dosage_form": "LIQUID", "product_ndc": "0869-0845", "generic_name": "Isopropyl Alcohol", "labeler_name": "Vi-Jon, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "70% Rubbing", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19890715", "listing_expiration_date": "20261231"}