Label: PAIN RELIEVING GEL- menthol gel
- NDC Code(s): 11822-8940-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 8, 2024
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- Active ingredient
- Purpose
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- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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- Other information
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Inactive ingredients
Aloe barbadensis leaf juice, Arctium lappa root extract, Arnica montana flower extract, blue 1, Boswellia carterii resin extract, Calendula officinalis flower extract, Camellia sinensis leaf extract, camphor, carbomer, Chamomilla recutita (matricaria) flower extract, glycerin, Ilex paraguariensis leaf extract, isopropyl alcohol, isopropyl myristate, Juniperus communis fruit extract, Melissa officinalis extract, silica, tocopheryl acetate, triethanolamine, water, yellow 5
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INGREDIENTS AND APPEARANCE
PAIN RELIEVING GEL
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-8940 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) FRANKINCENSE (UNII: R9XLF1R1WM) CHAMOMILE (UNII: FGL3685T2X) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CAMPHOR (NATURAL) (UNII: N20HL7Q941) ISOPROPYL ALCOHOL (UNII: ND2M416302) JUNIPER BERRY (UNII: O84B5194RL) MELISSA OFFICINALIS (UNII: YF70189L0N) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TROLAMINE (UNII: 9O3K93S3TK) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-8940-1 74 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 02/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2023 Labeler - Rite Aid (014578892) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11822-8940)