Label: NEURO MAX PAIN AND MUSCLE RELIEF GEL- methyl salicylate lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 69701-8623-5 - Packager: Starman Consulting LLC
- 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 June 23, 2015
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses:
- WARNINGS
- DO NOT USE
- PREGNANCY OR BREAST FEEDING
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients: Alcohol Denat, Althaea Officinalis (Marshmellow Root) Extract, Aphanizomenon Flos Aquae (Blue Green Algae) Extract, Avena Sativa (Oatstraw) Extract, Camellia Sinensis (Green Tea) Extract, Carbomer, Dimethyl Sulfone, Disodium EDTA, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Glycerin, Glycerol, Glycerol Dilaurate, Glyceryl Laurate, Hydroxypropyl Cellulose, PEG-8, Polysorbate 20, Potassium Laurate, Propylene Glycol, Propylene Glycol Dilaurate, Propylene Glycol Monolaurate, Silybum Marianum (Milk Thistle) Extract, Stellaria Media (Chickweed) Extract, Ulmus Rubra (Slippery Elm) Extract, Urtica Dioica (Nettle) Extract, Water.
- OTHER SAFETY INFORMATION
- QUESTIONS
- Neuro-Max-Pain-Muscle-Relief-Gel.jpg
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INGREDIENTS AND APPEARANCE
NEURO MAX PAIN AND MUSCLE RELIEF GEL
methyl salicylate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69701-8623 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 20 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 31 g in 100 g ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) .1 g in 100 g APHANIZOMENON FLOS-AQUAE (UNII: 49VG1X560X) .1 g in 100 g AVENA SATIVA LEAF (UNII: 206PI19V7R) .1 g in 100 g CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) .1 g in 100 g EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) .6 g in 100 g SILYBUM MARIANUM LEAF (UNII: K93P558418) .1 g in 100 g STELLARIA MEDIA LEAF (UNII: E6M924345X) .1 g in 100 g ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) .1 g in 100 g URTICA DIOICA LEAF (UNII: X6M0DRN46Q) .1 g in 100 g CARBOMER 940 (UNII: 4Q93RCW27E) .8 g in 100 g DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) 2.4 g in 100 g DISODIUM HEDTA (UNII: KME849MC7A) .05 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 9 g in 100 g GLYCERYL DILAURATE (UNII: MFL3ZIE8SK) 1 g in 100 g GLYCERYL LAURATE (UNII: Y98611C087) 1 g in 100 g HYDROXYPROPYL CELLULOSE (TYPE M) (UNII: U3JF91U133) 1 g in 100 g POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) 10 g in 100 g POLYSORBATE 20 (UNII: 7T1F30V5YH) 4.5 g in 100 g WATER (UNII: 059QF0KO0R) 16.85 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69701-8623-5 85 g in 1 TUBE; Type 0: Not a Combination Product 04/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/09/2015 Labeler - Starman Consulting LLC (079736006) Registrant - Starman Consulting LLC (079736006) Establishment Name Address ID/FEI Business Operations Cosmetic Solutions LLC 807907928 manufacture(69701-8623)
