Povidone Iodine

Product NDC: 69396-112
11-digit product format: 693960112
Labeler code: 69396
Product ID: 69396-112_29b3ae6b-a09b-f62c-e063-6294a90a150b
Type: HUMAN OTC DRUG
Nonproprietary name: Povidone Iodine 10%
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Trifecta Pharmaceuticals USA LLC
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-12-23
Substance: POVIDONE-IODINE
Active strength: 100 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Povidone Iodine
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
POVIDONE-IODINE	100 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
85H0HZU99M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
312563	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f80ccd8a-9b9b-bbf9-e053-6394a90ac827	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5f30b278-5791-4113-8781-878a9221ef8a	Product name	2	20230125
2a70c781-a755-4d76-b20a-a958acfbdcdc	Product name	2	20190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5	Product name	1	20180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22	Product name	1	20180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5c	Product name	1	20180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896	Product name	1	20170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99	Product name	1	20170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c	Product name	1	20150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69396-112-20	Povidone Iodine	1 in 1 BOX	OINTMENT	1		2
69396-112-20	Povidone Iodine	28.3 g in 1 TUBE	OINTMENT	28.3		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69396-112	POVIDONE IODINE (POVIDONE IODINE 10%) OINTMENT [TRIFECTA PHARMACEUTICALS USA LLC]	2	Current NDC, 2 package rows	20241222_f80ccd8a-9b9b-bbf9-e053-6394a90ac827.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 95 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3 OZ	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	b621b4cd-20db-44d8-b114-a977deea8eb4	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 0.5	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	c3a053ba-65fe-4540-9c81-29700cda5efa	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 3 OZ	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	2989afeb-8451-4a72-8456-195cd5117a41	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 1.25	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	17092ebf-8e57-4e1a-9bba-87a662c361c0	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 3	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	3ed3332e-f888-4b9c-aab7-99f8719b835e	2024-12-05	Warnings	Exact identifier application number: M003
OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZER	ETHYL ALCOHOL	Archer Manufacturing, Inc.	d05fbe85-26de-0d24-e053-2a95a90ab5cb	2024-12-05	Warnings	Exact identifier application number: M003
OPS AB ANTIBACTERIAL FOAMING	BENZALKONIUM CHLORIDE	Archer Manufacturing, Inc.	615921dd-46e5-403c-9ed3-f30beb0c0bb9	2024-12-05	Warnings	Exact identifier application number: M003
BLACK OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZER	ETHYL ALCOHOL	Archer Manufacturing, Inc.	d334b7f0-01dc-7f59-e053-2a95a90a06b5	2024-12-05	Warnings	Exact identifier application number: M003
BLACK OPS INSTANT HAND SANITIZER	BENZALKONIUM CHLORIDE	Archer Manufacturing, Inc.	d3366750-18b8-1194-e053-2995a90a4359	2024-12-05	Warnings	Exact identifier application number: M003
OPS RANCH HAND ANTIBACTERIAL FOAMING	CHLOROXYLENOL	Archer Manufacturing, Inc.	d8187090-8423-062e-e053-2a95a90aad18	2024-12-05	Warnings	Exact identifier application number: M003
BLACK OPS AB ANTIBACTERIAL FOAMING	BENZALKONIUM CHLORIDE	Archer Manufacturing, Inc.	d335bf6d-dc75-bd80-e053-2a95a90abb56	2024-12-05	Warnings	Exact identifier application number: M003
OPS INSTANT HAND SANITIZER	BENZALKONIUM CHLORIDE	Archer Manufacturing, Inc.	d4c65a93-832a-6a8b-e053-2a95a90a77b8	2024-12-05	Warnings	Exact identifier application number: M003
alcohol pad 01	ALCOHOL	Cosmuses Cosmetics (Ningbo) Co., Ltd.	03a6e8d4-535d-b316-e063-6294a90aebf5	2024-12-04	Warnings	Exact identifier application number: M003
antiseptic towelette 01	BENZALKONIUM CHLORIDE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	e9f2a1f1-ceb6-2f20-e053-2a95a90a18db	2024-12-04	Warnings	Exact identifier application number: M003
BobBarker antibacterial wrapped body	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	208b37b4-cfc3-4bf1-adc1-96d4b1d2cfa5	2024-12-04	Warnings	Exact identifier application number: M003
Walgreens 70% Isopropyl Alcohol	ISOPROPYL ALCOHOL	Walgreen Co.	21f125a0-73e8-34a9-e063-6294a90a8396	2024-12-04	Warnings	Exact identifier application number: M003
Emory Johns Creek Amenity	ALCOHOL AND SODIUM MONOFLUOROPHOSPATE	ASP Global	952ccb85-71bb-4d5d-ac9b-62851a39d36d	2024-12-04	Warnings	Exact identifier application number: M003
Watermelon Hand Sanitizer Spray. 01	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	1f0f9885-2ad5-09de-e063-6394a90ad0d7	2024-12-03	Warnings	Exact identifier application number: M003
Foster and Thrive Povidone-Iodine	POVIDONE IODINE	Strategic Sourcing Services, LLC	28621f29-ce45-c6dc-e063-6294a90aa5f7	2024-12-03	Warnings	Exact identifier application number: M003
Sanitizing Hand Mist Unscented	ETHYL ALCOHOL	ALO New York LLC	e194daee-2197-4718-e053-2a95a90a4890	2024-12-03	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
85H0HZU99M	POVIDONE-IODINE	25655-41-8	POVIDONE-IODINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312563	povidone-iodine 10 % Topical Ointment	PSN	f80ccd8a-9b9b-bbf9-e053-6394a90ac827	2
312563	povidone-iodine 0.1 MG/MG Topical Ointment	SCD	f80ccd8a-9b9b-bbf9-e053-6394a90ac827	2
312563	povidone-iodine 10 % (equal to 1 % available iodine) Topical Ointment	SY	f80ccd8a-9b9b-bbf9-e053-6394a90ac827	2
312563	povidone-iodine 10 % Topical Ointment	SY	f80ccd8a-9b9b-bbf9-e053-6394a90ac827	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
69396-112-20	69396011220	1 TUBE in 1 BOX (69396-112-20) / 28.3 g in 1 TUBE	1 tube	2022-12-23	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Globe Povidone Iodine USP 10%	Trifecta Pharmaceuticals USA LLC \| Trifecta Pharmaceuticals USA	2024-12-20	HUMAN OTC DRUG LABEL	2