Home NDC 63830-544 Ban-Aid
Product NDC 63830-544
11-digit product format 638300544
Labeler code 63830
Product ID 63830-544_518d209b-32b2-961b-e063-6294a90a09ce
Type HUMAN OTC DRUG
Nonproprietary name CHLOROXYLENOL
Dosage form SOAP
Route TOPICAL
Labeler Pro Chem, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2007-02-01
Substance CHLOROXYLENOL
Active strength 3 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product 63830-544 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63830-544 63830-544-14 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63830-544 63830-544-06 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 Ban-Aid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL 3 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0F32U78V2Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1860597 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63830-544-06 Ban-Aid 800 mL in 1 BAG SOAP 800 6 63830-544-06 Ban-Aid 1 in 1 BOX SOAP 1 6 63830-544-14 Ban-Aid 3785 mL in 1 BOTTLE, PLASTIC SOAP 3785 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CHLOROXYLENOL ACTIVE INGREDIENT 0F32U78V2Q BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 CHLOROXYLENOL ACTIVE MOIETY 0F32U78V2Q BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 COCO MONOISOPROPANOLAMIDE INACTIVE INGREDIENT 21X4Y0VTB1 BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 DECYL GLUCOSIDE INACTIVE INGREDIENT Z17H97EA6Y BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 FD&C YELLOW NO. 5 INACTIVE INGREDIENT I753WB2F1M BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 SODIUM LAURETH SULFATE INACTIVE INGREDIENT BPV390UAP0 BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63830-544 BAN-AID (CHLOROXYLENOL) SOAP [PRO CHEM, INC.] 4 Current NDC, Legacy NDC, 3 package rows 20250424_a251093c-77d1-4a2b-ba3d-e8768656cf6c.zip
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 9 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 Marketing end Sample Exclude flag Status 63830-544-06 63830054406 1 BAG in 1 BOX (63830-544-06) / 800 mL in 1 BAG 1 bag 2007-02-01 0000-00-00 No No Current 63830-544-14 63830054414 3785 mL in 1 BOTTLE, PLASTIC (63830-544-14) 3785 ml 2007-02-01 0000-00-00 No No Current