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		2026-10-23

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 111 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Povidone Iodine	POVIDONE IODINE GARGLE 0.5%	Humco Holding Group, Inc.	a7b9ad55-cfeb-6066-e053-2a95a90af975	2023-12-15	Warnings	Exact identifier application number: M003
Rite Aid Povidone Iodine	POVIDONE IODINE 10%	Rite Aid Corporation	5df6ff37-a4ea-d666-e053-2991aa0a9786	2023-12-15	Warnings	Exact identifier application number: M003
Rite Aid Decolorized Iodine	ETHYL ALCOHOL	Rite Aid Corporation	5e0d3664-b02a-ba28-e053-2991aa0a8a4c	2023-12-15	Warnings	Exact identifier application number: M003
De La Cruz Tincture of Iodine	IODINE AND SODIUM IODIDE AND ALCOHOL	DLC Laboratories, Inc.	5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b	2023-12-15	Warnings	Exact identifier application number: M003
ALCOHOL ANTISEPTIC HAND SANITIZER ANTIBACTERIAL	ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	0c73f4f5-2b1d-84ae-e063-6394a90a5d7b	2023-12-14	Warnings	Exact identifier application number: M003
TaeTu Aftercare	BENZALKONIUM CHLORIDE	Taetu LLC	dec15a4d-1a33-a78a-e053-2995a90a69fe	2023-12-14	Warnings	Exact identifier application number: M003
GNP Idoinde Tincture 2% Mild	IODINE AND SODIUM IODIDE AND ALCOHOL	Amerisource Bergen	32ad75b8-abd1-4151-a035-b6c9ae5fc888	2023-12-14	Warnings	Exact identifier application number: M003
Antibacterial Wet Wipes	BENZALKONIUM CHLORIDE	HangZhou YangYi Daily Cosmetics Technology Co., Ltd.	85d3914d-dbb8-5036-e053-2a91aa0a7cd4	2023-12-13	Warnings	Exact identifier application number: M003
AntiochPharma Rapidgel Hand Sanitizer	ALCOHOL	Weeks & Leo	0c57a9ea-de66-3ced-e063-6294a90a4b8d	2023-12-12	Warnings	Exact identifier application number: M003
antiseptic hand sanitizer 01	ALCOHOL	Cosmuses Cosmetics (Ningbo) Co., Ltd.	e9f9b7b6-fed7-10e1-e053-2a95a90a9aa6	2023-12-11	Warnings	Exact identifier application number: M003
AntiochPharma Hand Sanitizer	ALCOHOL	Weeks & Leo	a1a0d368-b004-59b8-e053-2995a90ab4b1	2023-12-11	Warnings	Exact identifier application number: M003
Septihol Hand Sanitizer	ALCOHOL	STERIS Corporation	279c5c6f-bf45-499f-a5a2-ddb535382146	2023-12-06	Warnings	Exact identifier application number: M003
Zany Antiseptic Gel	ALCOHOL	Laboratorios Zepol S.A.	ee085cb5-0ebf-498c-b622-b2c29d34bb9b	2023-12-01	Warnings	Exact identifier application number: M003
Prep Pad Sterile	POVIDONE-IODINE	Changzhou Maokang Medical Products Co., Ltd	758abf53-ad8a-62ac-e053-2991aa0a8f0c	2023-11-15	Warnings	Exact identifier application number: M003
FIRSTAR Alcohol Prep Pad	ISOPROPYL ALCOHOL	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	49a86020-b888-423f-99a5-02fa938105ec	2023-11-15	Warnings	Exact identifier application number: M003
CVS Health Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	CVS Health	4678074a-16f1-5480-e054-00144ff8d46c	2023-11-10	Warnings	Exact identifier application number: M003
Care One 70 Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Ahold U.S.A., Inc.	607b6917-2880-4b1c-83c6-f1297a828ecc	2023-11-10	Warnings	Exact identifier application number: M003
Topcare 3 Hydrogen Peroxide Wipes	HYDROGEN PEROXIDE	Topco Associates LLC	dc4b07b6-6476-4e32-901a-da8115d6a197	2023-11-10	Warnings	Exact identifier application number: M003
Topcare 70 Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Topco Associates LLC	bf9ee7da-69d9-47a2-8748-6b978ca3c298	2023-11-10	Warnings	Exact identifier application number: M003
MK Alcohol Swabstick Sterile	ISOPROPYL ALCOHOL	Changzhou Maokang Medical Products Co., Ltd	40c7cfc6-ef3b-4759-b9e9-6d7e1319a847	2023-11-09	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