Label: RECOVER HEMP POWERED TIDL- menthol 10.5% spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79740-002-02 - 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 January 17, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RECOVER HEMP POWERED TIDL
menthol 10.5% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79740-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10.5 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) CHAMOMILE (UNII: FGL3685T2X) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) ILEX PARAGUARIENSIS WHOLE (UNII: QJB02841ZY) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) JUNIPERUS COMMUNIS VAR. SAXATILIS FRUIT (UNII: G2UQA7N05B) WATER (UNII: 059QF0KO0R) HEMP (UNII: TD1MUT01Q7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79740-002-02 90 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/31/2020 Labeler - The Anthos Group (117511051) Establishment Name Address ID/FEI Business Operations Inspec Solutions LLC 081030372 manufacture(79740-002)
