NDC 72296-070 Tula Skincare Breakout Breakthrough Acne Toner Pads
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72296 - Tula Life Llc
- 72296-070 - Tula Skincare Breakout Breakthrough Acne Toner Pads
Product Packages
NDC Code 72296-070-01
Package Description: 1 JAR in 1 CARTON / 30 SWAB in 1 JAR
Product Details
What is NDC 72296-070?
What are the uses for Tula Skincare Breakout Breakthrough Acne Toner Pads?
Which are Tula Skincare Breakout Breakthrough Acne Toner Pads 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 Tula Skincare Breakout Breakthrough Acne Toner Pads 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NIACINAMIDE (UNII: 25X51I8RD4)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- LACTIC ACID (UNII: 33X04XA5AT)
- AZELAIC ACID (UNII: F2VW3D43YT)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PYRROLIDONE CARBOXYLIC ACID (UNII: 6VT1YZM21H)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- APPLE CIDER VINEGAR (UNII: 0UE22Q87VC)
- LACTOCOCCUS LACTIS (UNII: F1A0PSN10V)
- EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALLANTOIN (UNII: 344S277G0Z)
- CURCUMA LONGA WHOLE (UNII: W5488JUO8U)
- .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W)
- APPLE JUICE (UNII: 9871T0PD5P)
- CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85)
- PUNICA GRANATUM SEED (UNII: 7294Z34NS7)
- BEET JUICE (UNII: IOZ32L9H3O)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- LACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
- INULIN (UNII: JOS53KRJ01)
- CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- VANILLA PLANIFOLIA SEED (UNII: GKQ4MH0F2E)
- PINEAPPLE (UNII: 2A88ZO081O)
- ORANGE JUICE (UNII: 5A9KE2L9L3)
- CLOVE (UNII: K48IKT5321)
- SAGE (UNII: 065C5D077J)
What is the NDC to RxNorm Crosswalk for Tula Skincare Breakout Breakthrough Acne Toner Pads?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
* Please review the disclaimer below.
Patient Education
Salicylic Acid Topical
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.
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* 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".