i-Drops ARTIFICIAL TEARS

Product NDC: 73921-009
11-digit product format: 739210009
Labeler code: 73921
Product ID: 73921-009_6e2cfed9-0067-42dc-9de8-90f444d7ab62
Type: HUMAN OTC DRUG
Nonproprietary name: Hypromellose, Naphazoline Hydrochloride, Polysorbate 80, Zinc Sulfate
Dosage form: SOLUTION/ DROPS
Route: OPHTHALMIC
Labeler: GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Application: part349
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2021-04-01
Marketing end: 0000-00-00
Substance: HYPROMELLOSE, UNSPECIFIED; NAPHAZOLINE HYDROCHLORIDE; POLYSORBATE 80; ZINC SULFATE, UNSPECIFIED FORM
Active strength: 2 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73921-009-15	2023-02-08	C162847	48780-1	f386c649-f531-0266-e053-dadaa90a7c1a	03ae5fee-1901-44e5-b0b2-3c4311e44db1
73921-009-15	2023-01-30	C162847	48780-1	f386c649-f531-0266-e053-dadaa90a7c1a	03ae5fee-1901-44e5-b0b2-3c4311e44db1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3NXW29V3WO	HYPROMELLOSE, UNSPECIFIED	9004-65-3	HYPROMELLOSE, UNSPECIFIED
MZ1131787D	NAPHAZOLINE HYDROCHLORIDE	550-99-2	NAPHAZOLINE HYDROCHLORIDE
6OZP39ZG8H	POLYSORBATE 80	9005-65-6	POLYSORBATE 80
89DS0H96TB	ZINC SULFATE, UNSPECIFIED FORM		ZINC SULFATE, UNSPECIFIED FORM

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
73921-009-15	73921000915	1 BOTTLE, DROPPER in 1 CARTON (73921-009-15) > 15 mL in 1 BOTTLE, DROPPER	2021-04-01	0000-00-00	No	No	Current