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 32 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Universal Rubbing Alcohol	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	183efdc2-cf3e-4f06-b292-0cfd097418b3	2026-02-23	Warnings	Exact identifier application number: M003
Konix Povidone Iodine Topical Antiseptic	POVIDONE-IODINE	TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS	0cc6b001-4982-40ee-a476-151f86c14a8e	2026-02-19	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Save-A-Lot Food Stores Ltd	e279b23d-6779-4f04-a93c-1c2a49559639	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Meijer, Inc.	193292da-390b-4430-91b1-1d159ac50507	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Meijer, Inc.	4989f1cd-4555-405a-a5f8-8714d472983c	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Target Corporation	78693ec1-d725-408c-bb95-2261faad84ac	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M003
Travel Wipes Fresh Citrus Scent	ALCOHOL	SINGULAR ENTERPRISES LLC	ea77be5e-7c69-4787-b39a-4753b002dbbd	2026-02-18	Warnings	Exact identifier application number: M003
Travel Wipes Unscented	ISOPROPYL ALCOHOL	SINGULAR ENTERPRISES LLC	dd046146-fda7-438c-98ca-96ea1dd0ae0b	2026-02-18	Warnings	Exact identifier application number: M003
Benzalkonium chloride	FIRST AID ANTISEPTIC FOAM	Target Corporation	4599eb25-2877-fc62-e063-6294a90a5d18	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M003
Konix Povidone Iodine Topical Antiseptic	POVIDONE-IODINE	TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS	8a9848b0-19df-455a-9984-5ea2e5ce1b9f	2026-02-17	Warnings	Exact identifier application number: M003
Wintergreen 91 - Iron Lab	ETHYL ALCOHOL	Iron Lab SA de CV	323a0717-0d61-c911-e063-6394a90a4854	2026-02-17	Warnings	Exact identifier application number: M003
Ethyl Rubbing Alcohol	ALCOHOL	Iron Lab SA de CV	323b2f5d-34b9-8f5b-e063-6394a90a59d5	2026-02-17	Warnings	Exact identifier application number: M003
50 Ethyl Rubbing Alcohol	ALCOHOL	Iron Lab SA de CV	323b7ff8-91ce-c7a4-e063-6394a90a69fc	2026-02-17	Warnings	Exact identifier application number: M003
70 Alcohol Hand Sanitizer	ALCOHOL	Iron Lab SA de CV	323c06d5-c984-39b8-e063-6294a90a0d3f	2026-02-17	Warnings	Exact identifier application number: M003
50 Wintergreen Alcohol	ALCOHOL	Iron Lab SA de CV	323baeb1-e3ee-ec70-e063-6294a90a30f0	2026-02-17	Warnings	Exact identifier application number: M003
70 Rubbing Ethyl Alcohol	ALCOHOL	Iron Lab SA de CV	323be8b4-4588-e2a6-e063-6394a90ab68b	2026-02-17	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	United Natural Foods, Inc. dba UNFI	8a44aa29-58d6-4971-b572-4579f03ed227	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M003
INSTACLEAN HAND SANITIZING	ALCOHOL	SHIELD LINE LLC	6d606fae-d95e-cffc-e053-2991aa0a988b	2026-02-17	Warnings	Exact identifier application number: M003
Burn Cream	BENZALKONIUM CHLORIDE, LIDOCAINE HCI	Trifecta Pharmaceuticals USA LLC	087ac43c-1076-d1e2-e063-6294a90a5859	2026-02-16	Warnings	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Valu Merchandisers Company	a631c976-cb9b-4099-8630-2a10c14bd3bd	2026-02-16	Warnings, Adverse reactions	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