NDC 81120-103 Celesty Acne Series Instant Repair Mask
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81120 - Maba Kozmetik Limited Sirketi
- 81120-103 - Celesty
Product Packages
NDC Code 81120-103-01
Package Description: 1 TUBE in 1 BOX / 120 mL in 1 TUBE
Product Details
What is NDC 81120-103?
What are the uses for Celesty Acne Series Instant Repair Mask?
Which are Celesty Acne Series Instant Repair Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Celesty Acne Series Instant Repair Mask 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)
- BENTONITE (UNII: A3N5ZCN45C)
- PEG-30 CASTOR OIL (UNII: GF873K38RZ)
- TALC (UNII: 7SEV7J4R1U)
- KAOLIN (UNII: 24H4NWX5CO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ACACIA (UNII: 5C5403N26O)
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALMOND OIL (UNII: 66YXD4DKO9)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Celesty Acne Series Instant Repair Mask?
- RxCUI: 199632 - sulfur 3 % Topical Cream
- RxCUI: 199632 - sulfur 30 MG/ML Topical Cream
* 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".