PRO-SYS

Product NDC: 70275-201
11-digit product format: 702750201
Labeler code: 70275
Product ID: 70275-201_57dbfe25-5b60-3ad1-e063-6294a90a0a76
Type: HUMAN OTC DRUG
Nonproprietary name: Oral Wound Cleanser
Dosage form: LIQUID
Route: DENTAL
Labeler: Forward Science Technologies LLC
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-05-16
Substance: HYDROGEN PEROXIDE
Active strength: 15 mg/mL
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 · 21 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70275-201-16	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70275-201-28	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70275-201-16	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70275-201-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70275-201-16	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70275-201-28	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70275-201-16	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70275-201-28	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70275-201-16	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70275-201-28	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70275-201-16	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70275-201-28	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70275-201-16	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70275-201-28	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: PRO-SYS
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
HYDROGEN PEROXIDE	15 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
BBX060AN9V	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
205336	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
c357c8f8-6fd6-c2f8-e053-2995a90a4023	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
70275-201-16	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-16	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-16	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-03-25	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-16	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-16	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-16	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023
70275-201-28	2025-01-30	c357c8f8-6fd6-c2f8-e053-2995a90a4023

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70275-201-16	PRO-SYS	473 mL in 1 BOTTLE	LIQUID	473		6
70275-201-28	PRO-SYS	3785 mL in 1 BOTTLE	LIQUID	3785		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70275-201	OXISTOM (ORAL WOUND CLEANSER) LIQUID PRO-SYS (ORAL WOUND CLEANSER) LIQUID [FORWARD SCIENCE TECHNOLOGIES LLC]	4	Current NDC, Legacy NDC, 2 package rows	20250327_c357c8f8-6fd6-c2f8-e053-2995a90a4023.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 6 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AHLO PRO Healthy Gums	CETYLPYRIDINIUM CHLORIDE	Gervest USA Inc	4f5a0ccb-26e5-ebb6-e063-6394a90abbc5	2026-04-13	Warnings	Exact identifier application number: M022
Crest Scope Original Clean Mint	CETYLPYRIDINIUM CHLORIDE	The Procter & Gamble Manufacturing Company	4f1db6f4-acd7-a665-e063-6294a90a826b	2026-04-10	Warnings	Exact identifier application number: M022
Sore Throat	PHENOL GLYCERIN	Walgreens	1e845299-178e-49ce-9d08-7e9d548a5a6d	2026-04-09	Warnings	Exact identifier application number: M022
Sore throat cherry	PHENOL	Walgreens	67bed85e-e1e2-49ba-98d6-dfd4e1cd6856	2026-04-08	Warnings	Exact identifier application number: M022
Health-Tec Topical Anesthetic	BENZOCAINE	Dental Health Products, Inc.	5eb437c5-a2af-4c0d-b7b9-9ab7d093db85	2026-04-06	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	269b9e7f-c5c8-4023-a3ea-e39040ade271	2026-04-06	Warnings	Exact identifier application number: M022
Health-Tec Topical Anesthetic	BENZOCAINE	Dental Health Products, Inc.	c3fb6705-c647-4fe6-9aca-29735d01d8ea	2026-04-02	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	f061ec82-7f0e-4b93-afa6-ae9fe14ab4ea	2026-04-01	Warnings	Exact identifier application number: M022
CloSYS Silver Healthy Gums	CETYLPYRIDINIUM CHLORIDE	Rowpar Pharmaceuticals, Inc.	11fd3f31-ee0c-43d2-a856-929d1298277c	2026-04-01	Warnings	Exact identifier application number: M022
Crest Pro-Health Bold Fresh Breath	CETYLPYRIDINIUM CHLORIDE	The Procter & Gamble Manufacturing Company	5692c0ce-a914-08c4-e063-6394a90adf15	2026-04-01	Warnings	Exact identifier application number: M022
Anticavity Fluoride	SODIUM FLUORIDE AND ACIDULATED PHOSPHATE	Family Dollar (FAMILY WELLNESS)	1666fff6-9a8b-40f9-ae53-914152db386b	2026-04-01	Warnings	Exact identifier application number: M022
Sodium Chloride Normal Salt	SODIUM CHLORIDE	TWIN MED LLC	10230c8a-e5e5-44f1-b41d-80930899d6b9	2026-03-31	Warnings	Exact identifier application number: M022
Sootheez Birthday Cake	PECTIN	Primrose Candy Co.	4e5d8234-0521-0c8a-e063-6294a90ae62d	2026-03-31	Warnings	Exact identifier application number: M022
Sootheez Watermelon Mint	PECTIN	Primrose Candy Co.	4e5e4342-4647-ef25-e063-6394a90a1d13	2026-03-31	Warnings	Exact identifier application number: M022
PERIOGELX	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	4e5a67a0-f989-50df-e063-6394a90aae73	2026-03-31	Warnings	Exact identifier application number: M022
Periogel	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	1f9686b1-eac2-65b7-e063-6394a90a74fb	2026-03-31	Warnings	Exact identifier application number: M022
PERIOGELX	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	1f7ecd75-bb59-2f4f-e063-6294a90ace84	2026-03-31	Warnings	Exact identifier application number: M022
Baza Protect	ZINC OXIDE AND DIMETHICONE	Coloplast Corp	ed63df26-3879-46df-8e09-10be569b25be	2026-03-31	Warnings	Exact identifier application number: M022
Benzocaine 20%	BENZOCAINE 20%	PAI Holdings, LLC dba PAI Pharma	7fbce9a5-00dc-4a4a-8709-ab752bdf2f59	2026-03-25	Warnings	Exact identifier application number: M022
Kroger Extra Whitening	FLUORIDE	Kroger	e704c690-1383-4cd6-be85-28bdd9ff936b	2026-03-24	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
BBX060AN9V	HYDROGEN PEROXIDE	7722-84-1	HYDROGEN PEROXIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
205336	hydrogen peroxide 1.5 % Mucous Membrane Topical Solution	PSN	c357c8f8-6fd6-c2f8-e053-2995a90a4023	6
205336	hydrogen peroxide 15 MG/ML Mucous Membrane Topical Solution	SCD	c357c8f8-6fd6-c2f8-e053-2995a90a4023	6
205336	hydrogen peroxide 1.5 % Mucous Membrane Topical Solution	SY	c357c8f8-6fd6-c2f8-e053-2995a90a4023	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70275-201-16	70275020116	473 mL in 1 BOTTLE (70275-201-16)	473 ml	2022-05-16	0000-00-00	No	No	Current
70275-201-28	70275020128	3785 mL in 1 BOTTLE (70275-201-28)	3785 ml	2022-05-16	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
OxiStom - Forward Science Technologies LLC	Forward Science Technologies LLC	2026-07-30	HUMAN OTC DRUG LABEL	7