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NDC 11822-3322-09 Nicotine Polacrilex Gum 2 mg/1 Details

Nicotine Polacrilex Gum 2 mg/1

Nicotine Polacrilex Gum is a BUCCAL GUM, CHEWING in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid Corporation. The primary component is NICOTINE.

MedlinePlus Drug Summary

Nicotine chewing gum is used to help people stop smoking cigarettes. Nicotine chewing gum should be used together with a smoking cessation program, which may include support groups, counseling, or specific behavioral change techniques. Nicotine gum is in a class of medications called smoking cessation aids. It works by providing nicotine to your body to decrease the withdrawal symptoms experienced when smoking is stopped and as a substitute oral activity to reduce the urge to smoke.

Related Packages: 11822-3322-09
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Nicotine Gum

Product Information

NDC	11822-3322
Product ID	11822-3322_202f76af-0ef5-4e27-b194-b198c8379b13
Associated GPIs	97301000000000
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Nicotine Polacrilex Gum
Proprietary Name Suffix	n/a
Non-Proprietary Name	Nicotine Polacrilex
Product Type	HUMAN OTC DRUG
Dosage Form	GUM, CHEWING
Route	BUCCAL
Active Ingredient Strength	2
Active Ingredient Units	mg/1
Substance Name	NICOTINE
Labeler Name	Rite Aid Corporation
Pharmaceutical Class	Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA079044
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11822-3322-09 (11822332209)

Pricing Information	N/A
NDC Package Code	11822-3322-9
Billing NDC	11822332209
Package	100 BLISTER PACK in 1 CARTON (11822-3322-9) / 1 GUM, CHEWING in 1 BLISTER PACK
Marketing Start Date	2020-01-31
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 0e564f33-4781-4f91-a2ac-a76d927b250b Details

Drug Facts

Active ingredient (in each chewing piece) - 2 mg

Nicotine Polacrilex 2 mg (nicotine)

Purpose

Stop smoking aid

Use

reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking

Warnings

If you are pregnant or breast-feeding, only use this medicine on the advice of your health care provider. Smoking can seriously harm your child. Try to stop smoking without using any nicotine replacement medicine. This medicine is believed to be safer than smoking. However, the risks to your child from this medicine are not fully known.

Ask a doctor before use if you have

a sodium-restricted diet
heart disease, recent heart attack, or irregular heartbeat. Nicotine can increase your heart rate.
high blood pressure not controlled with medication. Nicotine can increase blood pressure.
stomach ulcer or diabetes
history of seizures

Ask a doctor or pharmacist before use if you are

using a non-nicotine stop smoking drug
taking prescription medicine for depression or asthma. Your prescription dose may need to be adjusted.

Stop use and ask a doctor if

mouth, teeth, or jaw problems occur
irregular heartbeat or palpitations occur
you get symptoms of nicotine overdose such as nausea, vomiting, dizziness, diarrhea, weakness, and rapid heartbeat
you have symptoms of an allergic reaction (such as difficulty breathing or rash)

Keep out of reach of children and pets.

Pieces of nicotine gum may have enough nicotine to make children and pets sick. Wrap used pieces of gum in paper and throw away in the trash. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions - 2 mg

if you are under 18 years of age, ask a doctor before use
before using this product, read the enclosed User's Guide for complete directions and other important information
begin using the gum on your quit day
if you smoke your first cigarette within 30 minutes of waking up, use 4 mg nicotine gum
if you smoke your first cigarette more than 30 minutes after waking up, use 2 mg nicotine gum according to the following 12 week schedule:

Weeks 1 to 6	Weeks 7 to 9	Weeks 10 to 12
1 piece every 1 to 2 hours	1 piece every 2 to 4 hours	1 piece every 4 to 8 hours

nicotine gum is a medicine and must be used a certain way to get the best results
chew the gum slowly until it tingles. Then park it between your cheek and gum. When the tingle is gone, begin chewing again until the tingle returns.
repeat this process until most of the tingle is gone (about 30 minutes)
do not eat or drink for 15 minutes before chewing the nicotine gum, or while chewing a piece
to improve your chances of quitting, use at least 9 pieces per day for the first 6 weeks
if you experience strong or frequent cravings, you may use a second piece within the hour. However, do not continuously use one piece after another since this may cause you hiccups, heartburn, nausea or other side effects.
do not use more than 24 pieces a day
it is important to complete treatment. If you feel you need to use the gum for a longer period to keep from smoking, talk to your health care provider.

Other information - 2 mg

each piece contains: calcium 115 mg, sodium 8 mg
store at 20 - 25ºC (68 - 77ºF)
protect from light

Inactive ingredients - 2 mg

acacia, acesulfame potassium, carnauba wax, FD&C blue #2 lake, FD&C red #40, FD&C yellow #6 lake, flavors, gum base, hydroxypropyl cellulose, magnesium oxide, sodium bicarbonate, sodium carbonate, sucralose, talc, titanium dioxide and xylitol.

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

PRINCIPAL DISPLAY PANEL - 2 mg

Compare to the active ingredient of Nicorette® Gum*

FREE | SUGAR

FROM | FREE

Nicotine Gum

Nicotine Polacrilex Gum USP,

2 mg (nicotine )

Stop Smoking Aid

FOR THOSE WHO SMOKE THEIR FIRST CIGARETTE MORE THAN 30 MINUTES AFTER WAKING UP

If you smoke your first cigarette WITHIN

30 MINUTES of waking up, use Nicotine Polacrilex Gum USP, 4 mg

COATED FRUIT FLAVOR

TO INCREASE YOUR SUCCESS IN QUITTING:

You must be motivated to quit.
Use Enough - Chew at least 9 pieces of Nicotine Polacrilex Gum per day during the first six weeks.
Use Long Enough - Use Nicotine Polacrilex Gum for the full 12 weeks.
Use with a Support Program as directed in the enclosed User's Guide.

Not for sale to those under 18 years of age.
Proof of age required.
Not for sale in vending machines or from any source where proof of age cannot be verified.

BLISTER PACKAGED FOR YOUR PROTECTION. DO NOT USE IF INDIVIDUAL SEAL ARE OPEN OR TORN.

*This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare, L,P., distributor or Nicorette® Gum.

DISTRIBUTED BY:

RITE AID, 30 HUNTER LANE,

CAMP HILL, PA 17011

www.riteaid.com

Package label

RITE AID Nicotine Gum Coated Fruit Flavor

INGREDIENTS AND APPEARANCE

NICOTINE POLACRILEX GUM

nicotine polacrilex gum, chewing

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11822-3322
Route of Administration	BUCCAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R)	NICOTINE	2 mg

Ingredient Name	Strength
Inactive Ingredients
ACACIA (UNII: 5C5403N26O)
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
CARNAUBA WAX (UNII: R12CBM0EIZ)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CARBONATE (UNII: 45P3261C7T)
SUCRALOSE (UNII: 96K6UQ3ZD4)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
XYLITOL (UNII: VCQ006KQ1E)

Product Characteristics
Color	brown (Light)	Score	no score
Shape	SQUARE	Size	14mm
Flavor	FRUIT	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11822-3322-9	100 in 1 CARTON	01/31/2020
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:11822-3322-3	20 in 1 CARTON	01/31/2020
2		1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA079044	01/31/2020

Labeler - Rite Aid Corporation (014578892)

Revised: 1/2022

Document Id: 202f76af-0ef5-4e27-b194-b198c8379b13

Set id: 0e564f33-4781-4f91-a2ac-a76d927b250b

Version: 4

Effective Time: 20220119