NDC 50157-612 Oatmeal Daily Moisturizing 8oz.
Dimethicone Lotion Topical
NDC Code 50157-612-22
Package Description: 227 g in 1 BOTTLE
What is NDC 50157-612?
The NDC code 50157-612 is assigned by the FDA to the product Oatmeal Daily Moisturizing 8oz. which is a human over the counter drug product labeled by Brands International. The generic name of Oatmeal Daily Moisturizing 8oz. is dimethicone. The product's dosage form is lotion and is administered via topical form. The product is distributed in a single package with assigned NDC code 50157-612-22 227 g in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.
What are the uses for Oatmeal Daily Moisturizing 8oz.?
This medication is used as a moisturizer to treat or prevent dry, rough, scaly, itchy skin and minor skin irritations (e.g., diaper rash, skin burns from radiation therapy). Emollients are substances that soften and moisturize the skin and decrease itching and flaking. Some products (e.g., zinc oxide, white petrolatum) are used mostly to protect the skin against irritation (e.g., from wetness). Dry skin is caused by a loss of water in the upper layer of the skin. Emollients/moisturizers work by forming an oily layer on the top of the skin that traps water in the skin. Petrolatum, lanolin, mineral oil and dimethicone are common emollients. Humectants, including glycerin, lecithin, and propylene glycol, draw water into the outer layer of skin. Many products also have ingredients that soften the horny substance (keratin) that holds the top layer of skin cells together (including urea, alpha hydroxy acids such as lactic/citric/glycolic acid, and allantoin). This helps the dead skin cells fall off, helps the skin keep in more water, and leaves the skin feeling smoother and softer.
What are Oatmeal Daily Moisturizing 8oz. Active Ingredients?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
Which are Oatmeal Daily Moisturizing 8oz. UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Oatmeal Daily Moisturizing 8oz.?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 891710 - dimethicone 1.3 % Topical Lotion
- RxCUI: 891710 - dimethicone 13 MG/ML Topical Lotion
Which are Oatmeal Daily Moisturizing 8oz. 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:
- VITAMIN E POLYETHYLENE GLYCOL SUCCINATE (UNII: O03S90U1F2)
- WATER (UNII: 059QF0KO0R)
- .BETA.-ELEOSTEARIC ACID (UNII: LA17B88161)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CARBOMER 1342 (UNII: 809Y72KV36)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
Which are the Pharmacologic Classes for Oatmeal Daily Moisturizing 8oz.?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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