Home NDC 73635-1218 Iodo Blanco (Iodine Tincture Decolorized)
Product NDC 73635-1218
11-digit product format 736351218
Labeler code 73635
Product ID 73635-1218_5d6cb4f5-8198-568a-e063-6294a90ac727
Type HUMAN OTC DRUG
Nonproprietary name Iodine 2%
Dosage form LIQUID
Route TOPICAL
Labeler Germa Products, LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-29
Substance ALCOHOL
Active strength 48 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Iodo Blanco (Iodine Tincture Decolorized)
Brand name suffix First Aid Antiseptic
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 48 mL/100mL
DailyMed Product Concepts# openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 44 of 115 · 2,286 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73635-1218-1 73635121801 30 mL in 1 BOTTLE, WITH APPLICATOR (73635-1218-1) 30 ml 2021-03-29 No No Current