NDC 71618-001 No Pain More Gain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71618 - Compes Cosmetic
- 71618-001 - No Pain More Gain
Product Packages
NDC Code 71618-001-01
Package Description: 100 mg in 1 PACKAGE
Product Details
What is NDC 71618-001?
What are the uses for No Pain More Gain?
Which are No Pain More Gain UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are No Pain More Gain Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
- PANTHENOL (UNII: WV9CM0O67Z)
- SQUALANE (UNII: GW89575KF9)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GALACTOARABINAN (UNII: SL4SX1O487)
- LEMON OIL (UNII: I9GRO824LL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- GOLD (UNII: 79Y1949PYO)
- PLATINUM (UNII: 49DFR088MY)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALCOHOL (UNII: 3K9958V90M)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- POLYAMINOPROPYL BIGUANIDE (UNII: 322U039GMF)
- CITRAL (UNII: T7EU0O9VPP)
- LINALOOL, (+)- (UNII: F4VNO44C09)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".