Ultracruz Antibacterial

Product NDC
49877-011
11-digit product format
498770011
Labeler code
49877
Product ID
49877-011_cc0e831d-9fa0-402c-9118-393376e65734
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
LOTION
Route
TOPICAL
Labeler
Cixi Zhixin Bird Clean-care Product Co., Ltd.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-08-22
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49877-011-012019-11-27C16284748780-19855e2a2-459f-60a7-e053-dbdaa90a05bdUltracruz Antibacteria Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49877-011-01Ultracruz AntibacterialNone237 mL in 1 BOTTLE, PLASTICLOTION2371

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49877-011ULTRACRUZ ANTIBACTERIAL NONE (BENZALKONIUM CHLORIDE) LOTION [CIXI ZHIXIN BIRD CLEAN-CARE PRODUCT CO., LTD.]1Legacy NDC, 1 package rows20140825_e3111c78-df33-419a-af35-294ea586b0d8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1102185benzalkonium chloride 0.1 % Topical LotionPSNe3111c78-df33-419a-af35-294ea586b0d81
1102185benzalkonium chloride 1 MG/ML Topical LotionSCDe3111c78-df33-419a-af35-294ea586b0d81
1102185benzalkonium chloride 0.1 % Topical LotionSYe3111c78-df33-419a-af35-294ea586b0d81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49877-011-0149877001101237 mL in 1 BOTTLE, PLASTIC237 mlHistorical