Liquid paraffin light 69.6% / Almond oil 30% bath oil
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2 branded products available
Part of the Infaderm brand family (generic: Liquid paraffin light + Almond oil)
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View all licensed products for Liquid paraffin light + Almond oil on the MHRA register
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 10 · 1992–2025
Showing the 50 most relevant studies, sorted by most relevant.
Bahjat Alhasso, Muhammad Usman Ghori, Barbara R. Conway
Scientia Pharmaceutica, 2022
R. B. Eldridge
Industrial & Engineering Chemistry Research, 1993
Tahere Khezeli, Ali Daneshfar, Reza Sahraei
Talanta, 2016
Elizabeth S. Budilarto, Afaf Kamal‐Eldin
European Journal of Lipid Science and Technology, 2015
R. Idem, S. Katikaneni, N. Bakhshi
Fuel Processing Technology, 1997
Liye Xia, Siyu Zhang, Zhiguang Guo
Advanced Materials Interfaces, 2023
Kengo Manabe, Takeshi Matsubayashi, Mizuki Tenjimbayashi, et al.
ACS nano, 2016
Aboubakar Gomna, Kokouvi Edem N’Tsoukpoe, Nolwenn Le Pierrès, et al.
Solar Energy Materials and Solar Cells, 2019
Ishaq Kariim, Hulda Swai, Thomas Kivevele
International Journal of Energy Research, 2023
A. Wollenberg, Sébastien Barbarot, A. Torrelo
International Journal of Dermatology, 2025
Xerosis cutis (dry skin) is a common and burdensome symptom of atopic dermatitis (AD). Topical emollients restore skin hydration and barrier function through the physicochemical properties of their nonactive constituents (e.g., glycerol, urea, lactic acid, liquid paraffin, petrolatum) and represent the mainstay of basic therapy for xerosis cutis associated with AD. Newer “emollients plus” containing active ingredients may expand the treatment options available to patients with AD; however, we believe that basic emollients remain an important strategy for the long‐term management of xerosis cutis. To that end, this article aims to review the clinical value of basic emollients for treating xerosis cutis in AD. We performed a series of literature searches to identify clinical studies of basic emollients containing one or more of the following ingredients: almond and coconut oils, amino acids, chondroitin, dexpanthenol, glucose, glycerol, glycosaminoglycans, hyaluronic acid, lactic acid, lanolin, olive oil, paraffin, petrolatum, phospholipids, polyunsaturated fatty acids, pyroglutamic acid, squalene, triglycerides, urea, vegetable oils, and vitamin E. From these searches, the authors identified articles of interest that described the efficacy of basic emollients for the treatment of xerosis cutis associated with AD. Studies included in our review varied widely in terms of sample size, study design, interventions, and endpoints but collectively showed that most basic emollient formulations are safe and effective at improving objective and subjective measures of xerosis cutis. These studies also demonstrated the importance of ongoing emollient therapy to avoid xerosis relapse and the additive benefits of emollients that combine ingredients with complementary biophysical properties (e.g., glycerol with its humectant effect plus petrolatum with its occludent effect). Overall, the current body of literature reinforces the role of basic emollients as effective and accessible treatment options for the long‐term management of xerosis cutis in patients with AD.
Abstract licence: CC BY
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.