NDC 70231-0017 Prep Everyday Clear Acne
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70231 - Prep Cosmetics Llc
- 70231-0017 - Prep Everyday Clear Acne
Product Packages
NDC Code 70231-0017-1
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 70231-0017?
What are the uses for Prep Everyday Clear Acne?
Which are Prep Everyday Clear Acne UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Prep Everyday Clear Acne 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:
- CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- GERANIUM MACULATUM ROOT OIL (UNII: H2E371EDYX)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- WATER (UNII: 059QF0KO0R)
- PROPANEDIOL (UNII: 5965N8W85T)
- PEG-12 GLYCERYL DIMYRISTATE (UNII: VS4W16AQ3X)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN (UNII: 9F8ET54T05)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- PEG-23 GLYCERYL DISTEARATE (UNII: 527412VE0U)
- SORBITOL (UNII: 506T60A25R)
- HYDROXYETHYL CELLULOSE (4000 CPS AT 1%) (UNII: ZYD53NBL45)
- MANDELIC ACID (UNII: NH496X0UJX)
- AZELAIC ACID (UNII: F2VW3D43YT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- SQUALANE (UNII: GW89575KF9)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Prep Everyday Clear Acne?
- RxCUI: 1047362 - salicylic acid 1 % Topical Solution
- RxCUI: 1047362 - salicylic acid 10 MG/ML Topical Solution
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[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".