NDC 73797-112 - Creme21 ultra protect travel kit

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
73797-112
Package NDCs from labels
73797-112-02
Manufacturer
Creme 21 GmbH
Effective date
2021-10-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Creme21 ultra protect travel kit - Creme 21 GmbHCreme 21 GmbH2021-10-22HUMAN OTC DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 112 of 232 · 4,634 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4x Medicated Severe Toothache and Gum GelBENZALKONIUM CHLORIDEMeijer97ce7890-5093-1763-e053-2a95a90afae72025-11-13WarningsExact identifier
unii: F5UM2KM3W7
4X Medicated Toothache and Gum GelBENZOCAINEWalmarta471a858-edbf-c31e-e053-2995a90a71562025-11-13WarningsExact identifier
unii: F5UM2KM3W7
4X Medicated Severe Toothache and Gum CreamBENZOCAINERite Aid996fdbeb-1fe3-77b6-e053-2995a90a25c72025-11-13WarningsExact identifier
unii: F5UM2KM3W7
Topco 4x Medicated Toothache and Gum GelBENZOCAINETopCareb463ea94-08a9-ca5d-e053-2a95a90a224b2025-11-13WarningsExact identifier
unii: F5UM2KM3W7
4X Medicated Severe Toothache and Gum GelBENZOCAINERite Aid99703bf4-f169-5e05-e053-2995a90afab42025-11-13WarningsExact identifier
unii: F5UM2KM3W7
Dial Antibacterial BarDIAL WHITE ANTIBACTERIAL BAR SOAPHenkel Corporation5691b718-bb66-1529-e054-00144ff88e882025-11-13WarningsExact identifier
unii: F5UM2KM3W7
Dial Complete Antibacterial Bar Spring WaterBENZALKONIUM CHLORIDEHenkel Corporationbd0db24a-668c-b9d0-e053-2a95a90aafbb2025-11-13WarningsExact identifier
unii: F5UM2KM3W7
Dr Lift Antibacterial Hand SanitizerETHYL ALCOHOLSpa de Soleilaba006cd-18db-e42f-e053-2995a90a46072025-11-12WarningsExact identifier
unii: 3K9958V90M
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
unii: 059QF0KO0R
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
unii: 059QF0KO0R
Meijer Hand Sanitizer Lemon SorbetALCOHOLShenzhen Lantern Scicence Co.,Ltd.434d3071-802b-f598-e063-6394a90a622d2025-11-11WarningsExact identifier
unii: 3K9958V90M
Meijer Hand Sanitizer Strawberry ShortcakeALCOHOLShenzhen Lantern Scicence Co.,Ltd.434d5f7c-f84d-d6f5-e063-6294a90aa6fe2025-11-11WarningsExact identifier
unii: 3K9958V90M
Walgreens Hand Sanitizer PearALCOHOLShenzhen Lantern Scicence Co.,Ltd.434ddef3-fe48-138d-e063-6394a90afc912025-11-11WarningsExact identifier
unii: 3K9958V90M
SunDrops 75ALCOHOLSunburst Chemicals, Inc.b0623424-939e-4b49-aa99-c1ef22cf0f2d2025-11-11WarningsExact identifier
unii: 3K9958V90M
SunDrops 77BENZALKONIUM CHLORIDESunburst Chemicals, Inc.fc0ba65c-5307-4251-a60b-cde84ad56ad82025-11-11WarningsExact identifier
unii: F5UM2KM3W7
SunDrops 87BENZALKONIUM CHLORIDESunburst Chemicals, Inc.584ea129-aaf2-402f-b9f1-3fec2a23a21c2025-11-11WarningsExact identifier
unii: F5UM2KM3W7
WhiskCare 375ALCOHOLWhisk Products, Inc.63c61968-73d7-4d31-9604-e56748b990fa2025-11-11WarningsExact identifier
unii: 3K9958V90M
Walgreens Hand Sanitizer Sweet PeaALCOHOLShenzhen Lantern Scicence Co.,Ltd.435ca082-0b6b-c55e-e063-6294a90af56e2025-11-11WarningsExact identifier
unii: 3K9958V90M
Smart Care Hand Sanitizer BarbieALCOHOLShenzhen Lantern Scicence Co.,Ltd.435d514e-204a-118b-e063-6294a90aa8a62025-11-11WarningsExact identifier
unii: 3K9958V90M
Smart Care Hand Sanitizer Spider-manALCOHOLShenzhen Lantern Scicence Co.,Ltd.435d939c-9bef-bf86-e063-6394a90a41422025-11-11WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.