CareTouch Alcohol-Free Foaming Hand Sanitizer

Product NDC
70393-456
11-digit product format
703930456
Labeler code
70393
Product ID
70393-456_86742494-dd74-40f4-95c8-44c3371e66ea
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Future Diagnostics Llc
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-03-01
Marketing end
2022-01-01
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70393-456-80ML - Milliliter70393-456128fc85b-8517-4d50-8849-a37f509092f812021-09-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70393-456-017039304560150 mL in 1 BOTTLE (70393-456-01) 50 ml2020-03-150000-00-00NoNoCurrent
70393-456-04703930456044 BOTTLE, PLASTIC in 1 BAG (70393-456-04) > 300 mL in 1 BOTTLE, PLASTIC (70393-456-25) 2019-03-010000-00-00NoNoCurrent
70393-456-08703930456088 BOTTLE in 1 PACKAGE (70393-456-08) > 50 mL in 1 BOTTLE (70393-456-01) 8 bottle2020-03-150000-00-00NoNoCurrent
70393-456-2570393045625300 mL in 1 BOTTLE, PLASTIC (70393-456-25) 300 ml2019-03-010000-00-00NoNoCurrent
70393-456-807039304568048 mL in 1 BOTTLE (70393-456-80) 48 ml2020-08-270000-00-00NoNoCurrent