Blue Green Foam

Product NDC: 70411-100
11-digit product format: 704110100
Labeler code: 70411
Product ID: 70411-100_fe1acb32-d100-4a47-b75d-1036c0d433ff
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: LIQUID
Route: TOPICAL
Labeler: H2Ocean, LLC
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-02-15
Substance: BENZALKONIUM CHLORIDE
Active strength: .13 g/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	70411-100	70411-100-08	D	Discontinued by firm		2026-10-16

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Blue Green Foam
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.13 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F5UM2KM3W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1020365	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
8627bf8b-2cce-45de-b37f-8478462645fa	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
70411-100-07	2021-12-10	BLUE GREEN FOAM
70411-100-08	2021-12-10	BLUE GREEN FOAM
70411-100-50	2021-12-10	BLUE GREEN FOAM
70411-100-07	2021-01-29	BLUE GREEN FOAM
70411-100-08	2021-01-29	BLUE GREEN FOAM
70411-100-50	2021-01-29	BLUE GREEN FOAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70411-100-07	Blue Green Foam	207 mL in 1 BOTTLE, PUMP	LIQUID	207	6
70411-100-08	Blue Green Foam	237 mL in 1 BOTTLE, PUMP	LIQUID	237	6
70411-100-09	Blue Green Foam	473 mL in 1 BOTTLE	LIQUID	473	6
70411-100-50	Blue Green Foam	50 mL in 1 BOTTLE, PUMP	LIQUID	50	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70411-100	BLUE GREEN FOAM (BENZALKONIUM CHLORIDE) LIQUID [H2OCEAN, LLC]	6	Current NDC, Legacy NDC, 4 package rows	20241102_8627bf8b-2cce-45de-b37f-8478462645fa.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 33 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
70%	ISOPROPYL ALCOHOL	Valu Merchandisers Company	be57aa83-f097-4ff8-81f8-13d731eea4e6	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Valu Merchandisers Company	81b5a92a-27a9-41d2-bc88-920833be6638	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Valu Merchandisers Company	8235b54f-2468-45ca-bff0-9149e582e886	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M003
Dealmed BZK Antiseptic Towelettes	BENZALKONIUM CHLORIDE	Dealmed Medical Supplies, LLC.	90a16a08-a7bf-418d-a95e-d735fb179a70	2026-02-16	Warnings	Exact identifier application number: M003
Iodine	IODINE	United Natural Foods, Inc. dba UNFI	8e840855-d210-4a99-b73f-6c69dcf2b6fb	2026-02-16	Warnings	Exact identifier application number: M003
IODDO IODINE	IODINE	EVI LABS	4af8552c-1f2b-84ad-e063-6394a90abb62	2026-02-16	Warnings	Exact identifier application number: M003
SaniiSwab	ETHYL ALCOHOL 62%	PolleyMed LLC	3b06f3a4-de7f-0d16-e063-6394a90af0dc	2026-02-14	Warnings	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Topco Associates LLC	e258fbd2-f1dd-4ba0-ac9b-64246f2db50b	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M003
Iodine Tincture	IODINE TINCTURE	Topco Associates LLC	e648f206-cc4f-4f5f-b31c-2fb8bf2708a7	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Topco Associates LLC	c3509fd3-e1bc-42bd-881e-7fb520ace9f9	2026-02-13	Warnings	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Walgreen Co.	b1c71ff1-8ffa-46df-9b43-86ed062c3a98	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M003
Iodine	IODINE	Walgreen Co.	d3d44c9f-4eb6-4e5b-9943-c0f80f06952d	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Walgreen Co.	eea239fe-554f-4487-9312-3ab0af27d530	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M003
Benzethonium chloride Plus Dyclonine hydrochloride	LIQUID BANDAGE	Chain Drug Consortium, LLC	d7154398-4f52-434a-b51b-b7829ccebf3b	2026-02-12	Warnings	Exact identifier application number: M003
Isopropyl alcohol	ISOPROPYL ALCOHOL	Medline Industries, LP	26e10080-d389-4994-e054-00144ff8d46c	2026-02-11	Warnings	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Medline Industries, LP	d980969d-694b-4c9e-a931-73beaceb51da	2026-02-11	Warnings	Exact identifier application number: M003
Isopropyl alcohol	ISOPROPYL ALCOHOL	Medline Industries, LP	2c85e3c0-2876-31c3-e054-00144ff88e88	2026-02-11	Warnings	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Medline Industries, LP	52a8b96e-dd4f-449e-b819-6f3ec5a27fb4	2026-02-11	Warnings	Exact identifier application number: M003
Hydrogen Peroxide First Aid Antiseptic	HYDROGEN PEROXIDE	Medline Industries, LP	4593f51a-9bcb-4149-9ce4-4f62183fd3dd	2026-02-11	Warnings	Exact identifier application number: M003
Hydrogen peroxide	HYDROGEN PEROXIDE	Medline Industries, LP	26a67a91-ee2d-6a6c-e054-00144ff88e88	2026-02-11	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	8627bf8b-2cce-45de-b37f-8478462645fa	6
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	8627bf8b-2cce-45de-b37f-8478462645fa	6
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	8627bf8b-2cce-45de-b37f-8478462645fa	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70411-100-07	70411010007	207 mL in 1 BOTTLE, PUMP (70411-100-07)	207 ml	2017-10-19	0000-00-00	No	No	Current
70411-100-08	70411010008	237 mL in 1 BOTTLE, PUMP	237 ml					Historical
70411-100-09	70411010009	473 mL in 1 BOTTLE (70411-100-09)	473 ml	2024-07-15		No	No	Current
70411-100-50	70411010050	50 mL in 1 BOTTLE, PUMP (70411-100-50)	50 ml	2016-02-15	0000-00-00	No	No	Current