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Search results for unoprostone root_names_stdName in Standardized Name (approximate match)
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2009)
Source URL:
First approved in 2009
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
O-Cymen-5-OL is an antifungal preservative used in cosmetics and beauty products to prevent harmful bacteria from developing and to prolong the shelf-life of formulas. It is part of the Isopropyl Cresols family and is originally developed synthetically in the form of a crystal. O-Cymen-5-OL is also used as a cosmetic biocide, or ingredient that helps to cleanse the skin or to prevent odor by destroying or inhibiting the growth of microorganisms, according to research. O-Cymen-5-OL is approved by the FDA for use as a direct and indirect food additive and has been approved by the CIR for use in cosmetics up to .5% concentration. However, in the European Union, it is only approved for use up to .1%. Studies in Japan, some dating back to 1956, found O-Cymen-5-OL to be neurotoxic in animals and have led to heavier restrictions on its use in cosmetics there. O-Cymen-5-OL (Dekasol BL) is used in oral care, to fight periodontal disease.
Status:
Possibly Marketed Outside US
Source:
ANDA072781
(2009)
Source URL:
First approved in 2009
Source:
ANDA072781
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Sodium isobutoxide is an alkoxide of isobutanol. It is used in organic chemistry for the synthesis of isobutyl ethers.
Status:
Possibly Marketed Outside US
Source:
ANDA078233
(2007)
Source URL:
First approved in 2007
Source:
ANDA078233
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
M006
(2020)
Source URL:
First approved in 2006
Source:
M032
Source URL:
Class (Stereo):
CHEMICAL (EPIMERIC)
Status:
Possibly Marketed Outside US
Source:
Volu-Firm Night Treatment with Retinol
Source URL:
First approved in 2004
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2000)
Source URL:
First approved in 2000
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2009)
Source URL:
First approved in 2000
Source:
21 CFR 333E
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Possibly Marketed Outside US
First approved in 2000
Source:
Excel by United Pet Group
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Isopropyl Myristate is a synthetic oil used as an emollient, thickening agent or lubricant in beauty products. Isopropyl Myristate is a popular cosmetic and pharmaceutical ingredient. It is most often used as an additive in aftershaves, shampoos, bath oils, antiperspirants, deodorants, oral hygiene products, and various creams and lotions.
Status:
Possibly Marketed Outside US
Source:
M017
(1995)
Source URL:
First approved in 1995
Source:
M017
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Isopropyl Stearate is an ester of isopropyl alcohol and stearic acid that used as binder, emollient, and moisturizer in the pharmaceutical and cosmetic industries. Stearate esters act primarily as lubricants on the skin's surface, which gives the skin a soft and smooth appearance. Isopropyl Stearate has the unique properties of low viscosity and oily nature, which results in a nongreasy, hydrophobic film when applied to the skin or lips. Undiluted Isopropyl Stearate was classified as a slight ocular irritant.
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(1994)
Source URL:
First approved in 1994
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)