Nicorette White Ice Mint is a Oral Gum, Chewing in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Nicotine.
Product ID | 0135-0474_1107242e-6fb9-48c7-a01a-f299b1c90177 |
NDC | 0135-0474 |
Product Type | Human Otc Drug |
Proprietary Name | Nicorette White Ice Mint |
Generic Name | Nicotine Polacrilex |
Dosage Form | Gum, Chewing |
Route of Administration | ORAL |
Marketing Start Date | 2009-06-29 |
Marketing Category | NDA / NDA |
Application Number | NDA018612 |
Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
Substance Name | NICOTINE |
Active Ingredient Strength | 2 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2009-06-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-08-01 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-06-29 |
Marketing End Date | 2014-06-27 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-06-29 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-29 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-29 |
Marketing End Date | 2016-01-31 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-06-29 |
Marketing End Date | 2018-08-01 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-09-01 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-29 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-29 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-12-03 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-07-09 |
Marketing End Date | 2014-11-21 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-06-29 |
Marketing End Date | 2018-08-01 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-06-29 |
Marketing End Date | 2014-11-21 |
Marketing Category | NDA |
Application Number | NDA018612 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-29 |
Ingredient | Strength |
---|---|
NICOTINE | 2 mg/1 |
SPL SET ID: | 673fd19f-69b3-4f73-b9b4-18b5f4cbf69c |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0135-0475 | Nicorette White Ice Mint | Nicorette White Ice Mint |
0135-0474 | Nicorette White Ice Mint | Nicorette White Ice Mint |
0113-0704 | basic care nicotine | Nicotine polacrilex |
0113-0713 | basic care nicotine | Nicotine Polacrilex |
0113-0749 | basic care nicotine | Nicotine Polacrilex |
0113-0761 | basic care nicotine | Nicotine Polacrilex |
0113-7007 | basic care nicotine | Nicotine Polacrilex |
0113-7008 | basic care nicotine | nicotine polacrilex |
0113-7029 | basic care nicotine | Nicotine Polacrilex |
0113-0029 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0053 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0170 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0206 | good sense nicotine | Nicotine Polacrilex |
0113-0344 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0422 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0456 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0532 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0734 | Good Sense Nicotine | Nicotine Polacrilex |
0113-0854 | Good Sense Nicotine | Nicotine polacrilex |
0113-0873 | good sense nicotine | Nicotine Polacrilex |
0113-0957 | Good Sense Nicotine | Nicotine Polacrilex |
0113-1125 | Good Sense Nicotine | Nicotine Polacrilex |
0113-1190 | good sense nicotine | Nicotine Polacrilex |
0113-1352 | good sense nicotine | Nicotine Polacrilex |
0113-6000 | Tru Relief Nicotine | Nicotine Polacrilex |
0113-6001 | Tru Relief Nicotine | Nicotine Polacrilex |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NICORETTE 97148669 not registered Live/Pending |
GlaxoSmithKline Consumer Healthcare, L.P. 2021-11-30 |
NICORETTE 97148654 not registered Live/Pending |
GlaxoSmithKline Consumer Healthcare, L.P. 2021-11-30 |
NICORETTE 97076449 not registered Live/Pending |
GlaxoSmithKline Consumer Healthcare, L.P. 2021-10-15 |
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GLAXOSMITHKLINE CONSUMER HEALTHCARE L.P. 2000-09-20 |
NICORETTE 77006854 3509141 Live/Registered |
GlaxoSmithKline Consumer Healthcare L.P. 2006-09-25 |
NICORETTE 75185006 2103431 Dead/Cancelled |
SmithKline Beecham Consumer Healthcare,L.P. 1996-10-17 |
NICORETTE 75185005 2103430 Dead/Cancelled |
SmithKline Beecham Consumer Healthcare,L.P. 1996-10-17 |
NICORETTE 73264072 1186363 Live/Registered |
AB Leo 1980-05-29 |
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