HICELl

Product NDC
75768-0003
11-digit product format
757680003
Labeler code
75768
Product ID
75768-0003_b2ff0252-6913-23c2-e053-2995a90a5f7b
Type
HUMAN OTC DRUG
Nonproprietary name
L-ascorbic acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
ORGANELLE Inc
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-11-01
Marketing end
0000-00-00
Substance
ASCORBIC ACID
Active strength
5 g/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75768-0003-12023-01-30C16284748780-1f386c64a-0dbd-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75768-0003-1HICELl100 mL in 1 BOTTLELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75768-0003HICELL (L-ASCORBIC ACID) LIQUID [ORGANELLE INC]1Legacy NDC, 1 package rows20201101_b2ff3cb7-d12e-f385-e053-2a95a90ac3b0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75768-0003-175768000301100 mL in 1 BOTTLE (75768-0003-1) 100 ml2020-11-010000-00-00NoNoCurrent