Label: ELGIN PAIN RELIEF- menthol gel
- NDC Code(s): 30056-004-28, 30056-004-32
- Packager: Eco-Logics, Inc.
- Category: HUMAN OTC DRUG LABEL
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 May 9, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- OTC-ACTIVE INGREDIENT SECTION
- Purpose
- Uses
- Warning
- Directions
- Ask doctor before use if you:
-
When using this product
When using this product:
Avoid contact with the eyes or mucous membranes.
Do not apply to wounds or damaged skin.
Do not use with other ointments, creams, sprays or linaments.
Do nopt apply to irrated skin or ifexcessive irration develops.
Do not bandage.
Wash hands after use with cool water.
Do not use with heating pad or device.
- Stop Use and Ask a Doctor if:
- Keep out of reach of children:
- Directions
- Other information
- Inactive Ingredients
- If pregnant or breast feeding:
- Principle Dislay Panel
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INGREDIENTS AND APPEARANCE
ELGIN PAIN RELIEF
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30056-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 35 mg in 1 g Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) METHYLPARABEN (UNII: A2I8C7HI9T) TROLAMINE (UNII: 9O3K93S3TK) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) ALOE VERA LEAF (UNII: ZY81Z83H0X) ISOPROPYL ALCOHOL (UNII: ND2M416302) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30056-004-28 3780 g in 1 JUG; Type 0: Not a Combination Product 07/11/2016 2 NDC:30056-004-32 877 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/11/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/11/2016 Labeler - Eco-Logics, Inc. (047667022) Registrant - Elginex Corporation (005142799) Establishment Name Address ID/FEI Business Operations Natural Essentials,Inc. 947484713 manufacture(30056-004)