LADY GOONG

Product NDC: 80766-0005
11-digit product format: 807660005
Labeler code: 80766
Product ID: 80766-0005_b23944f7-f8bf-b2a4-e053-2a95a90a1b87
Type: HUMAN OTC DRUG
Nonproprietary name: Ethylhexylglycerin
Dosage form: LIQUID
Route: VAGINAL
Labeler: Lady House Co., Ltd.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-10-17
Marketing end: 0000-00-00
Substance: ETHYLHEXYLGLYCERIN
Active strength: 1 g/100g
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
80766-0005-1	2022-01-28	C162847	48780-1	d6a99b39-b2a9-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80766-0005-1	LADY GOONG	1.6 g in 1 APPLICATOR	LIQUID	1.6		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80766-0005	LADY GOONG (ETHYLHEXYLGLYCERIN) LIQUID [LADY HOUSE CO., LTD.]	1	Legacy NDC, 1 package rows	20201022_b23944f7-f8c0-b2a4-e053-2a95a90a1b87.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
80766-0005-1	80766000501	1.6 g in 1 APPLICATOR (80766-0005-1)	1.6 g	2020-10-17	0000-00-00	No	No	Current