Label: EVELS SECRET NATURAL PAIN RELIEF DAREDEVIL STRENGTH- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 66902-090-01, 66902-090-02, 66902-090-03, 66902-090-04, view more66902-090-05, 66902-090-08, 66902-090-16, 66902-090-28 - Packager: NATURAL ESSENTIALS, INC.
- 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 February 25, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
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Warnings:
Use only as directed.
- - For external use only.
- - 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.
- - Avoid contact with eyes or mucous membranes.
- Directions:
- Inactive ingredients
- Principal Display Panel - 4 oz. Container Label
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INGREDIENTS AND APPEARANCE
EVELS SECRET NATURAL PAIN RELIEF DAREDEVIL STRENGTH
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66902-090 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) MAGNESIUM SULFATE (UNII: DE08037SAB) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BORATE (UNII: 91MBZ8H3QO) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66902-090-04 118.29 mL in 1 CONTAINER; Type 0: Not a Combination Product 2 NDC:66902-090-05 14.79 mL in 1 CONTAINER; Type 0: Not a Combination Product 3 NDC:66902-090-01 29.57 mL in 1 CONTAINER; Type 0: Not a Combination Product 4 NDC:66902-090-02 59.15 mL in 1 CONTAINER; Type 0: Not a Combination Product 5 NDC:66902-090-03 88.72 mL in 1 CONTAINER; Type 0: Not a Combination Product 6 NDC:66902-090-08 236.59 mL in 1 CONTAINER; Type 0: Not a Combination Product 7 NDC:66902-090-16 473.18 mL in 1 CONTAINER; Type 0: Not a Combination Product 8 NDC:66902-090-28 3785.41 mL in 1 CONTAINER; 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 part348 11/15/2014 Labeler - NATURAL ESSENTIALS, INC. (947484713) Establishment Name Address ID/FEI Business Operations NATURAL ESSENTIALS, INC. 947484713 MANUFACTURE(66902-090)