FDA.reportPublic FDA data

Dr.Jucre Rebirth Activating Toner

Product NDC
83071-020
11-digit product format
830710020
Labeler code
83071
Product ID
83071-020_ff0ae282-1f6c-441a-a7dd-863b46931dc2
Type
HUMAN OTC DRUG
Nonproprietary name
Betaine
Dosage form
LIQUID
Route
TOPICAL
Labeler
NATURECELL CO., LTD.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2022-10-01
Substance
BETAINE
Active strength
.001 g/100mL
Pharmacologic classes
Methylating Activity [MoA], Methylating Agent [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr.Jucre Rebirth Activating Toner
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BETAINE.001 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3SCV180C9W

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83071-020-01Dr.Jucre Rebirth Activating Toner150 mL in 1 BOTTLELIQUID1501
83071-020-02Dr.Jucre Rebirth Activating Toner1 in 1 CARTONLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83071-020DR.JUCRE REBIRTH ACTIVATING TONER (BETAINE) LIQUID [NATURECELL CO., LTD.]1Current NDC, Legacy NDC, 2 package rows20221108_7f333594-d672-4259-83ae-5d591e620f0d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
83071-020-0183071002001150 mL in 1 BOTTLE150 mlHistorical
83071-020-02830710020021 BOTTLE in 1 CARTON (83071-020-02) / 150 mL in 1 BOTTLE (83071-020-01) 1 bottle2022-10-010000-00-00NoNoCurrent