Label: DR. SPENSERS NATURAL HERBAL PAIN RELIEF- menthol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69562-022-01 - Packager: LTC Health Corp
- 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 16, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Keep out of reach of children
- Indications:
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Warnings:
For external use ONLY. If rash or irritation occurs, discontinue use. The application of eternal heat such as an electric heating pad may result in excessive skin irritation or skin burn. Avoid contact with eyes, mucous membranes, and damaged skin or open wound. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.
- Do not use
- Directions:
- Non-medicinal Ingredients:
- Dr. Spenser's Product Label
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INGREDIENTS AND APPEARANCE
DR. SPENSERS NATURAL HERBAL PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69562-022 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 2.625 g in 75 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) ELEUTHERO (UNII: ZQH6VH092Z) PERSICARIA TINCTORIA LEAF (UNII: FU6582QMPV) TERMINALIA CHEBULA FRUIT (UNII: S8R4V700NK) TARAXACUM OFFICINALE (UNII: 39981FM375) ISOPROPYL ALCOHOL (UNII: ND2M416302) SUNFLOWER OIL (UNII: 3W1JG795YI) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM HYDROXIDE (UNII: 55X04QC32I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYSORBATE 60 (UNII: CAL22UVI4M) PEG-150 STEARATE (UNII: 7BSG7DF10Q) STEARETH-20 (UNII: L0Q8IK9E08) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69562-022-01 75 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 11/01/2009 Labeler - LTC Health Corp (202782066) Registrant - LTC Health Corp (202782066) Establishment Name Address ID/FEI Business Operations LTC Health Corp 202782066 manufacture(69562-022)
