Povidone Iodine

Product NDC: 68786-140
Requested package NDC: 68786-140-01
11-digit product format: 687860140
Labeler code: 68786
Product ID: 68786-140_47e7d21f-e345-6413-e063-6294a90aa9be
Type: HUMAN OTC DRUG
Nonproprietary name: POVIDONE-IODINE
Dosage form: SWAB
Route: TOPICAL
Labeler: Sion Biotext Medical Ltd
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-04-17
Substance: POVIDONE-IODINE
Active strength: .1 g/1
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	68786-140	68786-140-01	I	Inactivated by FDA		excluded / ndc_excluded.zip	`9bebd1f3094a…`	`5416666fcb17…`

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: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
POVIDONE-IODINE	.1 g/1

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
797730	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
3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	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

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2020-11-18	Povidone Iodine Prep Pad
2020-11-18	Povidone Iodine Prep Pad
2020-01-31	Povidone Iodine Prep Pad
2020-01-31	Povidone Iodine Prep Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68786-140-01	Povidone Iodine	10 in 1 CASE	SWAB	10		6
68786-140-01	Povidone Iodine	100 in 1 BOX	SWAB	100		6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
POVIDONE-IODINE	ACTIVE INGREDIENT	85H0HZU99M	POVIDONE IODINE (POVIDONE-IODINE) SWAB [SION BIOTEXT MEDICAL LTD]	1
IODINE	ACTIVE MOIETY	9679TC07X4	POVIDONE IODINE (POVIDONE-IODINE) SWAB [SION BIOTEXT MEDICAL LTD]	1
NONOXYNOL-9	INACTIVE INGREDIENT	48Q180SH9T	POVIDONE IODINE (POVIDONE-IODINE) SWAB [SION BIOTEXT MEDICAL LTD]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	POVIDONE IODINE (POVIDONE-IODINE) SWAB [SION BIOTEXT MEDICAL LTD]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68786-140	POVIDONE IODINE (POVIDONE-IODINE) SWAB [SION BIOTEXT MEDICAL LTD]	5	Current NDC, Legacy NDC, 2 package rows	20240125_3ef9a05b-e434-4f6d-94a1-94aa6723fe8f.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 94 of 114 · 2,270 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Instant Hand Antiseptic	ALCOHOL	ASP Global	9aca3f89-cdde-430c-8eb6-43a3ac3fc0df	2024-12-06	Warnings	Exact identifier application number: M003
Instant Hand Antiseptic	BENZALKONIUM CHLORIDE	ASP Global	4eef4b0f-9209-45a4-8a0e-7891fc380fe5	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 1.5	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	2998b2bd-6208-4cb4-982b-0ffb97d7d75d	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 0.5	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	68003c71-5959-476f-b252-1f131e9305e2	2024-12-05	Warnings	Exact identifier application number: M003
MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3	BENZETHONIUM CHLORIDE	Yangzhou H&R Plastic Daily Chemical Co., Ltd.	e35e468a-1f0c-4a3f-ac6a-cd55a72f3cc2	2024-12-05	Warnings	Exact identifier application number: M003
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

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
797730	povidone-iodine 10 % Medicated Pad	PSN	3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	6
797730	povidone-iodine 100 MG/ML Medicated Pad	SCD	3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	6
797730	povidone-iodine 10 % (titratable iodine 1 % ) Medicated Pad	SY	3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	6
797730	povidone-iodine 10 % Medicated Pad	SY	3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	6
797730	povidone-iodine 10 % Medicated Swabstick	SY	3ef9a05b-e434-4f6d-94a1-94aa6723fe8f	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68786-140-01	68786014001	10 BOX in 1 CASE (68786-140-01) / 100 PACKET in 1 BOX / 1 SWAB in 1 PACKET	10 box	2013-04-17	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Povidone Iodine Prep Pad	Sion Biotext Medical Ltd \| Sion Biotext Mexico SAPI de CV	2026-01-08	HUMAN OTC DRUG LABEL	6