Royal 70-percent Alcohol Foam Hand Sanitizer

Product NDC
70415-202
11-digit product format
704150202
Labeler code
70415
Product ID
70415-202_d4b84637-e6ce-29ce-e053-2995a90a4285
Type
HUMAN OTC DRUG
Nonproprietary name
ETHYL ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
CWGC LA Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-02-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70415-202-01Royal 70-percent Alcohol Foam Hand Sanitizer1000 mL in 1 BOTTLELIQUID100010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70415-202ROYAL 70-PERCENT ALCOHOL FOAM HAND SANITIZER (ETHYL ALCOHOL) LIQUID [CWGC LA INC.]10Legacy NDC, 1 package rows20231214_bc650f09-3539-4cb9-8f56-332090d2bc39.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616805ethanol 70 % Topical FoamPSNbc650f09-3539-4cb9-8f56-332090d2bc3910
616805ethanol 0.7 ML/ML Topical FoamSCDbc650f09-3539-4cb9-8f56-332090d2bc3910
616805ethanol 70 % Topical FoamSYbc650f09-3539-4cb9-8f56-332090d2bc3910

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70415-202-01704150202011000 mL in 1 BOTTLE (70415-202-01) 1000 ml2016-02-010000-00-00NoNoCurrent