MIRACLE WATER 3 in 1

Product NDC: 79659-001
11-digit product format: 796590001
Labeler code: 79659
Product ID: 79659-001_ecd762dd-3b61-40eb-845e-a8d996cfe832
Type: HUMAN OTC DRUG
Nonproprietary name: Potassium hydroxide
Dosage form: SPRAY
Route: TOPICAL
Labeler: ORIGIN G&B CO.,LTD
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-07-16
Marketing end: 0000-00-00
Substance: POTASSIUM HYDROXIDE
Active strength: 0 mg/mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79659-001-01	2022-01-28	C162847	48780-1	d6a99b39-c5c1-a426-e053-dadaa90af4c2	MIRACLE WATER 3 in 1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79659-001-01	MIRACLE WATER 3 in 1	400 mL in 1 PACKAGE	SPRAY	400		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79659-001	MIRACLE WATER 3 IN 1 (POTASSIUM HYDROXIDE) SPRAY [ORIGIN G&B CO.,LTD]	1	Legacy NDC, 1 package rows	20200728_80ecc609-4ad8-4391-8af8-e65c85772419.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
79659-001-01	79659000101	400 mL in 1 PACKAGE (79659-001-01)	400 ml	2020-07-16	0000-00-00	No	No	Current