Label: TIDL PAIN RELIEF MASSAGING ROLL-ON- roll-on liniment
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Contains inactivated NDC Code(s)
NDC Code(s): 79740-011-01, 79740-011-02 - Packager: The Anthos Group
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 October 26, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TIDL PAIN RELIEF MASSAGING ROLL-ON
roll-on linimentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79740-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.5 g in 100 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength SIALYL LEWIS A (UNII: ZEJ6FM4UJK) GINGER (UNII: C5529G5JPQ) CROCUS SATIVUS FLOWER (UNII: 00IF91KFKQ) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) ETHYL VANILLIN (UNII: YC9ST449YJ) WATER (UNII: 059QF0KO0R) BORNEOL (UNII: M89NIB437X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79740-011-02 85 g in 1 BOTTLE; Type 0: Not a Combination Product 10/26/2022 2 NDC:79740-011-01 85 g in 1 BOTTLE; Type 0: Not a Combination Product 10/26/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/26/2022 Labeler - The Anthos Group (117511051) Establishment Name Address ID/FEI Business Operations THE ANTHOS GROUP 117511051 manufacture(79740-011)