NDC 72805-030 Mychelle Dermaceuticals Replenishing Solar Defense Spf 30 Broad Spectrum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72805 - French Transit, Ltd.
- 72805-030 - Mychelle Dermaceuticals Replenishing Solar Defense
Product Packages
NDC Code 72805-030-77
Package Description: 1 TUBE in 1 BOX / 68 mL in 1 TUBE
Product Details
What is NDC 72805-030?
What are the uses for Mychelle Dermaceuticals Replenishing Solar Defense Spf 30 Broad Spectrum?
Which are Mychelle Dermaceuticals Replenishing Solar Defense Spf 30 Broad Spectrum UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mychelle Dermaceuticals Replenishing Solar Defense Spf 30 Broad Spectrum 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN (UNII: 9F8ET54T05)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- BARLEY (UNII: 5PWM7YLI7R)
- MACADAMIA OIL (UNII: 515610SU8C)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- SANDALWOOD (UNII: 3641YW25N2)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MALIC ACID, L- (UNII: J3TZF807X5)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- ALCOHOL (UNII: 3K9958V90M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DOCOSANOL (UNII: 9G1OE216XY)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".