NDC 70631-034 Lavaderm After Sun For Pain And Itching
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70631 - Young Living Essential Oils, Lc
- 70631-034 - Lavaderm After Sun
Product Packages
NDC Code 70631-034-25
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 57 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 70631-034?
What are the uses for Lavaderm After Sun For Pain And Itching?
Which are Lavaderm After Sun For Pain And Itching UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
Which are Lavaderm After Sun For Pain And Itching 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:
- DOCOSANOL (UNII: 9G1OE216XY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PICEA MARIANA LEAF OIL (UNII: Q1J49L1A5O)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- WATER (UNII: 059QF0KO0R)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- JOJOBA OIL (UNII: 724GKU717M)
- POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERYL MONOUNDECYLENATE (UNII: IK8A76Q5G8)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)
- PHYTATE SODIUM (UNII: 88496G1ERL)
What is the NDC to RxNorm Crosswalk for Lavaderm After Sun For Pain And Itching?
- RxCUI: 1314935 - menthol 0.5 % Topical Spray
- RxCUI: 1314935 - menthol 5 MG/ML Topical Spray
* 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".