Hi-IQ Hand Sanitizer

Product NDC
76701-350
11-digit product format
767010350
Labeler code
76701
Product ID
76701-350_c5efade7-98e6-2cfa-e053-2995a90a6923
Type
HUMAN OTC DRUG
Nonproprietary name
Hi-IQ Water
Dosage form
SPRAY
Route
TOPICAL
Labeler
Hand Sanitizer LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-06-18
Marketing end
0000-00-00
Substance
HYDROGEN CATION
Active strength
10 mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76701-350-01Hi-IQ Hand Sanitizer50.275 mL in 1 BOTTLE, PUMPSPRAY50.2753
76701-350-16Hi-IQ Hand Sanitizer473.176 mL in 1 BOTTLE, SPRAYSPRAY473.1763
76701-350-28Hi-IQ Hand Sanitizer3785.41 mL in 1 BOTTLESPRAY3785.413

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76701-350HI-IQ HAND SANITIZER (HI-IQ WATER) SPRAY [HAND SANITIZER LLC]3Legacy NDC, 3 package rows20210630_c50ca22c-1893-a257-e053-2995a90ad37f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76701-350-017670103500150.275 mL in 1 BOTTLE, PUMP (76701-350-01) 50.275 ml2021-06-180000-00-00NoNoCurrent
76701-350-1676701035016473.176 mL in 1 BOTTLE, SPRAY (76701-350-16) 473.176 ml2021-06-180000-00-00NoNoCurrent
76701-350-28767010350283785.41 mL in 1 BOTTLE (76701-350-28) 3785.41 ml2021-06-180000-00-00NoNoCurrent