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NDC 11673-0434-12 Tartar control plus .92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL Details

Tartar control plus .92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL

Tartar control plus is a ORAL MOUTHWASH in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL.

Product Information

NDC	11673-0434
Product ID	11673-434_80dff5a1-d1b2-4c6b-a996-9409319e704e
Associated GPIs	90750030000932
GCN Sequence Number	005789
GCN Sequence Number Description	salicylic acid LIQUID 17 % TOPICAL
HIC3	L5A
HIC3 Description	KERATOLYTICS
GCN	22811
HICL Sequence Number	002465
HICL Sequence Number Description	SALICYLIC ACID
Brand/Generic	Generic
Proprietary Name	Tartar control plus
Proprietary Name Suffix	n/a
Non-Proprietary Name	Eucalyptol, menthol, methyl salicylate, thymol
Product Type	HUMAN OTC DRUG
Dosage Form	MOUTHWASH
Route	ORAL
Active Ingredient Strength	.92; .42; .6; .64
Active Ingredient Units	mg/mL; mg/mL; mg/mL; mg/mL
Substance Name	EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Labeler Name	Target Corporation
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part356
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11673-0434-12 (11673043412)

Pricing Information	N/A
NDC Package Code	11673-434-12
Billing NDC	11673043412
Package	1499 mL in 1 BOTTLE, PLASTIC (11673-434-12)
Marketing Start Date	2014-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 3f83d630-3df6-4dfe-9d4e-afc55d2f4c17 Details

Active ingredients

Eucalyptol 0.092%

Menthol 0.042%

Methyl salicylate 0.060%

Thymol 0.064%

Purpose

Antigingivitis, antiplaque

Use

help control plaque that leads to gingivitis

Warnings

for this product

Do not use

if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease.

Stop use and ask a dentist if

gingivitis, bleeding, or redness persists for more than 2 weeks.

Keep out of reach of children.

If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out; do not swallow

children 6 years to under 12 years of age - supervise use

children under 6 years of age - do not use

this rinse is not intended to replace brushing or flossing

Other information

cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-86°F)

Inactive ingredients

water, alcohol 21.6%, sorbitol, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, flavor, sodium saccharin, blue 1

Disclaimer

This product is not manufactured or distribted by Johnson & Johnson Healthcare Products, distributor of Listerine Ultraclean With Everfresh Technology - Artic Mint.

Adverse Reactions

Dist. by Targert Corp., Mpls., MN 55403

2015 Target Brands, Inc.,

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Empty and

Replace Cap

PLASTIC

BOTTLE

how2recycle.info

DSP-TN-15000

DSP-M-34

SDS-TN-15012

principal display panel

SAFETY SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

antiseptic

mouthwash

antigingivitis/antiplaque

Compare to active ingredients in Listerine ultraclean with Everfresh Technology-Artic Mint

helps fight tartar build up

fights plaque & gingivits

freshens Breath

up & up

mint

flavor

50.7 FL OZ (1.5 L)

INGREDIENTS AND APPEARANCE

TARTAR CONTROL PLUS

eucalyptol, menthol, methyl salicylate, thymol mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-434
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK)	EUCALYPTOL	0.92 mg in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.42 mg in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	0.60 mg in 1 mL
THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E)	THYMOL	0.64 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SORBITOL (UNII: 506T60A25R)
POLOXAMER 407 (UNII: TUF2IVW3M2)
BENZOIC ACID (UNII: 8SKN0B0MIM)
ZINC CHLORIDE (UNII: 86Q357L16B)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11673-434-12	1499 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part356	05/01/2014

Labeler - Target Corporation (006961700)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(11673-434)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(11673-434)

Revised: 6/2022

Document Id: 80dff5a1-d1b2-4c6b-a996-9409319e704e

Set id: 3f83d630-3df6-4dfe-9d4e-afc55d2f4c17

Version: 13

Effective Time: 20220609