oido sana
Generic: isopropyl alcohol
Labeler: promex llcDrug Facts
Product Profile
Brand Name
oido sana
Generic Name
isopropyl alcohol
Labeler
promex llc
Dosage Form
SOLUTION
Routes
Active Ingredients
isopropyl alcohol .95 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
58988-1100
Product ID
58988-1100_fd1d6b7b-081c-4b49-95f2-4a5650c9d188
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M014
Listing Expiration
2026-12-31
Marketing Start
2006-05-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
589881100
Hyphenated Format
58988-1100
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
oido sana (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
M014 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .95 g/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (58988-1100-1) / 30 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["AURICULAR (OTIC)"], "spl_id": "fd1d6b7b-081c-4b49-95f2-4a5650c9d188", "openfda": {"unii": ["ND2M416302"], "rxcui": ["631799"], "spl_set_id": ["71e84695-49e8-459f-ac5e-118b5235fe06"], "manufacturer_name": ["ProMex LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (58988-1100-1) / 30 mL in 1 BOTTLE, PLASTIC", "package_ndc": "58988-1100-1", "marketing_start_date": "20060531"}], "brand_name": "OIDO SANA", "product_id": "58988-1100_fd1d6b7b-081c-4b49-95f2-4a5650c9d188", "dosage_form": "SOLUTION", "product_ndc": "58988-1100", "generic_name": "ISOPROPYL ALCOHOL", "labeler_name": "ProMex LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OIDO SANA", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": ".95 g/mL"}], "application_number": "M014", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060531", "listing_expiration_date": "20261231"}