Label: MEN-PHOR- menthol, camphor lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 54162-550-02, 54162-550-07, 54162-550-09 - Packager: Geritrex 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 January 17, 2018
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Uses
- Directions
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Warnings
For External Use Only
• Avoid contact with eyes. If contact occurs,
rinse eyes thoroughly with water.
• If improvement does not occur, or condition
worsens after regular use as directed,
discontinue use and consult a physician.
• Do not use on children under two years of age.
• Do not apply under compresses or bandages - Other Ingredient
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEN-PHOR
menthol, camphor lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54162-550 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.11 g in 222 mL CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 1.11 g in 222 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) STEARIC ACID (UNII: 4ELV7Z65AP) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) CETYL ALCOHOL (UNII: 936JST6JCN) DMDM HYDANTOIN (UNII: BYR0546TOW) GLYCOL STEARATE (UNII: 0324G66D0E) PEG-200 DILAURATE (UNII: TWV5J70L88) PEG-40 CASTOR OIL (UNII: 4ERD2076EF) PETROLATUM (UNII: 4T6H12BN9U) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54162-550-07 222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/31/2015 2 NDC:54162-550-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/31/2015 3 NDC:54162-550-09 222 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 07/31/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/31/2015 Labeler - Geritrex LLC (112796248) Establishment Name Address ID/FEI Business Operations Geritrex LLC 112796248 manufacture(54162-550)