HYDRO H

Product NDC
69422-5001
11-digit product format
694225001
Labeler code
69422
Product ID
69422-5001_61840956-ea63-4855-b862-223d6327a39d
Type
HUMAN OTC DRUG
Nonproprietary name
ARBUTIN
Dosage form
SOLUTION
Route
TOPICAL
Labeler
General Bio Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-12-09
Marketing end
0000-00-00
Substance
ARBUTIN
Active strength
3 mg/mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69422-5001-12020-01-31C16284748780-19d75b9d0-eacd-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69422-5001-1HYDRO H20 mL in 1 BOTTLESOLUTION201

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARBUTINACTIVE INGREDIENTC5INA23HXFHYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1
ARBUTINACTIVE MOIETYC5INA23HXFHYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1
HYALURONIC ACIDINACTIVE INGREDIENTS270N0TRQYHYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1
PREZATIDE COPPERINACTIVE INGREDIENT6BJQ43T1I9HYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1
WATERINACTIVE INGREDIENT059QF0KO0RHYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69422-5001HYDRO H (ARBUTIN) SOLUTION [GENERAL BIO CO., LTD.]1Legacy NDC, 1 package rows20141209_9c25650d-a3c6-45f0-bff9-3b1d9df46d60.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69422-5001-16942250010120 mL in 1 BOTTLE20 mlHistorical