GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE

Product NDC: 49283-110
11-digit product format: 492830110
Labeler code: 49283
Product ID: 49283-110_453f35fe-71ec-6476-e063-6394a90ace8c
Type: HUMAN OTC DRUG
Nonproprietary name: BENZALKONIUM CHLORIDE
Dosage form: LOTION
Route: TOPICAL
Labeler: CHEMCO CORPORATION
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-01-19
Marketing end: 2027-12-31
Substance: BENZALKONIUM CHLORIDE
Active strength: .1 g/100g
NDC exclude flag: No
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 · 18 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	49283-110-07	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	49283-110-07	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	49283-110-07	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	49283-110-07	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	49283-110-07	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	49283-110-07	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	49283-110-07	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	49283-110-07	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	49283-110-07	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: GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.1 g/100g

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
1102185	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
f2a107aa-5ad3-7bad-e053-2a95a90a1d97	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49283-110-07	2025-12-05	C162847	48780-1	2cef2736-6dea-d83d-e063-dadaa90ab31f	49283-110-07
49283-110-07	2025-01-30	C162847	48780-1	2cef2736-6dea-d83d-e063-dadaa90ab31f	49283-110-07

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49283-110-07	GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE	20 g in 1 POUCH	LOTION	20		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49283-110	GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE (BENZALKONIUM CHLORIDE) LOTION [CHEMCO CORPORATION]	2	Current NDC, 1 package rows	20230922_f2a107aa-5ad3-7bad-e053-2a95a90a1d97.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 39 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand sanitizer	HAND SANITIZER SPRAY	Beimei Biotechnology (Guangzhou) Co., Ltd.	49455156-1072-14f5-e063-6294a90abdff	2026-01-26	Warnings	Exact identifier application number: M003
Anti-bacterial Hand Wipes	ANTI-BACTERIAL HAND WIPES	Jinhua Aidi Daily Chemical Co., Ltd.	494b09a4-4982-13bf-e063-6394a90a486f	2026-01-26	Warnings	Exact identifier application number: M003
Homworks Alcohol Wipes Multipurpose	ETHYL ALCOHOL	Acadian Crossing Consumer Products, LLC.	c9f0c3b3-5f39-dfa6-e053-2995a90a7644	2026-01-26	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	87288939-cc34-4437-94ab-dcb997d6acd5	2026-01-23	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	10454042-ff2e-44ce-b2e2-436cc004897f	2026-01-23	Warnings	Exact identifier application number: M003
Everlit Survival Sting Relief Pad	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	3a0414ea-f862-aa0f-e063-6294a90aecb7	2026-01-23	Warnings	Exact identifier application number: M003
Medline	POVIDONE-IODINE	Medline Industries, LP	48ebfdd6-d346-7e26-e063-6394a90af11a	2026-01-23	Warnings	Exact identifier application number: M003
EVERLIT SURVIVAL IODINE PREP PADS	POVIDONE-IODINE	EVERLIT GLOBAL INC.	3a03fc8d-2653-9183-e063-6294a90ad76e	2026-01-23	Warnings	Exact identifier application number: M003
EVERLIT SURVIVAL PREP PAD	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	3a03ed81-5b1d-172e-e063-6394a90ac59c	2026-01-23	Warnings	Exact identifier application number: M003
Everlit Survival Antiseptic Wipe	ANTISEPTIC WIPE	EVERLIT GLOBAL INC.	3a03f7e6-cc74-22a2-e063-6394a90a5f9f	2026-01-23	Warnings	Exact identifier application number: M003
Rite Aid Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Rite Aid	bca837b0-5044-4e97-e053-2a95a90a13af	2026-01-22	Warnings	Exact identifier application number: M003
Drs. Pharmacy Triple Antibiotic AND BURN RELIEF	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	OL PHARMA TECH, LLC Drs PHARMACY	4928d9dd-542b-fe8b-e063-6294a90a9252	2026-01-22	Warnings	Exact identifier application number: M003
DOP Ethyl Alcohol 70%	ETHYL ALCOHOL	Omega & Delta Co., Inc.	b96d85f8-739c-4b96-9dd5-8119ebf66c9f	2026-01-21	Warnings	Exact identifier application number: M003
AshleyBelle Moisturizing Hand Sanitizer Rose Lychee	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	48dfcbe1-8e0c-1715-e063-6394a90a733f	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Swabstick	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	977b6077-bf47-4e02-bde4-c752e73d7628	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Scrub	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	000bf57b-1805-4746-bf1c-32856241213a	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Solution	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	6946eb98-6870-4b21-9dda-b01a8adab84b	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Prep Pad	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	e561332d-e419-43db-a68e-0c0d49b01c9a	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povindone Iodine Swabstick	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	2610fde4-4572-4d15-a970-f6d3beb734fe	2026-01-21	Warnings	Exact identifier application number: M003
Lights Povidone Iodine Solution	POVIDONE-IODINE	Lights Medical Manufacture Co., Ltd.	7d4a92be-0601-4256-bc5b-bc1b07d97bb7	2026-01-21	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
1102185	benzalkonium chloride 0.1 % Topical Lotion	PSN	f2a107aa-5ad3-7bad-e053-2a95a90a1d97	3
1102185	benzalkonium chloride 1 MG/ML Topical Lotion	SCD	f2a107aa-5ad3-7bad-e053-2a95a90a1d97	3
1102185	benzalkonium chloride 0.1 % Topical Lotion	SY	f2a107aa-5ad3-7bad-e053-2a95a90a1d97	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49283-110-07	49283011007	20 g in 1 POUCH (49283-110-07)	20 g	2023-01-19	2027-12-31	No	No	Historical