Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
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NDC Code(s):
11822-0664-1,
11822-0664-2,
11822-0664-3,
11822-0664-4, view more11822-0664-5, 11822-0664-7
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 19, 2022
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use
- Stop use
- Keep out of reach of children.
- Directions
- Other infromation
- Inactive ingredients
- ADA council Statement
- Disclaimer
- Adverse Reactions
- principal display panel
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INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0664 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0664-1 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 2 NDC:11822-0664-2 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 3 NDC:11822-0664-3 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 4 NDC:11822-0664-4 94 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 5 NDC:11822-0664-5 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 6 NDC:11822-0664-7 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/21/1995 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 07/21/1995 Labeler - Rite Aid (014578892) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11822-0664) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11822-0664)