Hand Sanitizer Pure Experience Gel

Product NDC
70956-311
11-digit product format
709560311
Labeler code
70956
Product ID
70956-311_ab6c7f82-7c4c-41ee-bce0-38921f69bd24
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Absara Cosmetics S.A.P.I DE C.V.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-06-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70956-311-017095603110160 mL in 1 BOTTLE (70956-311-01) 60 ml2020-06-010000-00-00NoNoCurrent
70956-311-0270956031102100 mL in 1 BOTTLE (70956-311-02) 100 ml2020-06-010000-00-00NoNoCurrent
70956-311-0370956031103250 mL in 1 BOTTLE (70956-311-03) 250 ml2020-06-010000-00-00NoNoCurrent
70956-311-0470956031104500 mL in 1 BOTTLE (70956-311-04) 500 ml2020-06-010000-00-00NoNoCurrent
70956-311-0570956031105700 mL in 1 BOTTLE (70956-311-05) 700 ml2020-06-010000-00-00NoNoCurrent
70956-311-06709560311061000 mL in 1 BOTTLE (70956-311-06) 1000 ml2020-06-010000-00-00NoNoCurrent
70956-311-07709560311071.5 mL in 1 BAG (70956-311-07) 1.5 ml2020-06-010000-00-00NoNoCurrent
70956-311-08709560311083780 mL in 1 BOTTLE (70956-311-08) 3780 ml2020-06-010000-00-00NoNoCurrent