Hyaluronic Acid Gel

Product NDC
70663-001
11-digit product format
706630001
Labeler code
70663
Product ID
70663-001_3178d496-2d9b-470d-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Hyaluronate
Dosage form
GEL
Route
TOPICAL
Labeler
Meso System S.A.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-04-15
Marketing end
0000-00-00
Substance
HYALURONATE SODIUM
Active strength
4 mg/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70663-001-022020-01-31C16284748780-19d75b9d0-77c8-f424-e053-dadaa90a57ceHyaluronic Acid Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70663-001-01Hyaluronic Acid Gel50 mL in 1 BOTTLE, PLASTICGEL501
70663-001-02Hyaluronic Acid Gel1 in 1 BOTTLE, PLASTICGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70663-001HYALURONIC ACID GEL (SODIUM HYALURONATE) GEL [MESO SYSTEM S.A.]1Legacy NDC, 2 package rows20160427_317888dc-c04d-3e0e-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70663-001-017066300010150 mL in 1 BOTTLE, PLASTIC50 mlHistorical
70663-001-02706630001021 in 1 BOTTLE, PLASTICHistorical