NDC 70592-020-01 - Freeze 24 7 Intense Hydrating Face Mask

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
70592-020
Requested NDC
70592-020-01
Package NDCs from labels
70592-020-01, 70592-020-02
Manufacturer
Summit C&T LLC | SANSUNG LIFE & SCIENCE CO., LTD.
Effective date
2016-04-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Witch Hazel - Summit C&T LLC | SANSUNG LIFE & SCIENCE CO., LTD.Summit C&T LLC | SANSUNG LIFE & SCIENCE CO., LTD.2016-04-07HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70592-020-022020-01-31C16284748780-19d75b9d0-1f9c-f424-e053-dadaa90a57ceccbb55a9-2ee5-4698-9cc0-ba00c1e6529e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70592-020-01Freeze 24 7 Intense Hydrating Face Mask30 mL in 1 CELLO PACKPATCH301
70592-020-02Freeze 24 7 Intense Hydrating Face Mask1 in 1 CARTONPATCH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70592-020FREEZE 24 7 INTENSE HYDRATING FACE MASK (WITCH HAZEL) PATCH [SUMMIT C&T LLC]1Legacy NDC, 2 package rows20160407_ccbb55a9-2ee5-4698-9cc0-ba00c1e6529e.zip

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 15 of 15 · 282 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
65af6684-efe0-4713-86b5-a92d151af842ccbb55a9-2ee5-4698-9cc0-ba00c1e6529e2016-04-07WarningsExact identifier
spl id: 65af6684-efe0-4713-86b5-a92d151af842
spl set id: ccbb55a9-2ee5-4698-9cc0-ba00c1e6529e

Reported adverse events (FAERS/openFDA)#

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