NDC 62111-0211 Moisturizing Lip Balmspf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62111 - Akg Innovations Llc
- 62111-0211 - Moisturizing Lip Balmspf30
Product Packages
NDC Code 62111-0211-3
Package Description: 1 TUBE in 1 BOX / 4.3 g in 1 TUBE
Product Details
What is NDC 62111-0211?
What are the uses for Moisturizing Lip Balmspf30?
Which are Moisturizing Lip Balmspf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Moisturizing Lip Balmspf30 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SHEA BUTTER (UNII: K49155WL9Y)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- ARGAN OIL (UNII: 4V59G5UW9X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALOE VERA FLOWER (UNII: 575DY8C1ER)
- LEVOMENOL (UNII: 24WE03BX2T)
- CURCUMA LONGA LEAF (UNII: H2HC4RY52C)
- LAWSONIA INERMIS FLOWERING TOP (UNII: UF2093XE64)
- AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)
- OCIMUM TENUIFLORUM TOP (UNII: 34T63W8ULS)
- COCCINIA GRANDIS FRUIT (UNII: VLJ6WOT3K5)
- CORALLINA OFFICINALIS (UNII: 4004498D06)
- CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP)
- JOJOBA OIL (UNII: 724GKU717M)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- MENTHOL (UNII: L7T10EIP3A)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".