Sweet skin Hand sanitizer

Product NDC
80958-001
11-digit product format
809580001
Labeler code
80958
Product ID
80958-001_d479ef31-c4d6-56c8-e053-2995a90a0cb0
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
GEL
Route
TOPICAL
Labeler
Sweet Skin Etc. Llc
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-10-20
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
1 g/L
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
80958-001-01Sweet skin Hand sanitizer3.785 L in 1 BOTTLEGEL3.7853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80958-001SWEET SKIN HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [SWEET SKIN ETC. LLC]3Legacy NDC, 1 package rows20230214_b215a83c-5aba-e5d3-e053-2a95a90a2ca9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSNb215a83c-5aba-e5d3-e053-2a95a90a2ca93
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCDb215a83c-5aba-e5d3-e053-2a95a90a2ca93
1049228benzalkonium chloride 0.1 % Topical GelSYb215a83c-5aba-e5d3-e053-2a95a90a2ca93

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80958-001-01809580001013.785 L in 1 BOTTLE (80958-001-01) 3.785 l2020-10-200000-00-00NoNoCurrent