vaseline album (Brataco, Indonesia), stearic acid 
(Brataco, Indonesia), cetyl alcohol (Brataco, 
Indonesia), thrietanolamin (Brataco, Indonesia), 
dimeticon (Brataco, Indonesia), methyl paraben 
(Brataco, Indonesia), propylene glycol (Brataco, 
Indonesia), ethanol 0% (pharmaceutical grade), 
ethanol 35% (pharmaceutical grade), etanol 70% 
(pharmaceutical grade), and aquadest. The 
instruments that was used were oven (Binder, ED 
115/Esv 00-17289), rotary evaporator (Heidolph, 
Germany), analitical balance (Wiggen Hauser), 
waterbath (Memert, Germany), pH meter (WTW 
82362 Weilheim, Germany), termometer, 
sentrifugator (PLC-series), vacuum pump (Rotary 
Vane), viskometer Rheosys Merlin VR, freeze dryer 
(Virtis, United States), the equipment of adhesivity, 
the equioment of spreadability and glassware (Pyrex, 
United States).  
2.2 Methods 
2.2.1 Extraction of Moringa oleifera Leaf 
Extract of leaves Moringa oleifera leaves was 
obtained by using maceration method. The 
maceration method was performed with a ratio of 
1:40. The 10 grams of dried sample powder was 
extracted by using of 400 mL ethanol 70% 
pharmaceutical grade for 72 hours at room 
temperature. After that, it was filtered with filter 
paper and vacuum pump. The extract was 
evaporated by using rotary evaporator and was 
continued by using waterbath until dry (Vongsak et 
al., 2013).  
The extract of moringa leaf was obtained by 
maceration method with ethanol 70%. This is based 
on research results of Vongsak et al. (2013) which 
indicates that the nutritious compounds of phenolic 
and flavonoids as antioxidants can be maximized by 
using the methods. This study will be identify the 
specific and non-specific parameters of moringa leaf 
extract. 
2.2.2  Specification of Extract 
The levels of β-carotene in moringa leaf extract was 
determined by using High Performance Liquid 
Chromatography. The extracts were also identified 
for their chemical content, the extract specification 
test included water content, total ash content, acid 
soluble ash content. 
2.2.3 Formulation of Moringa oleifera 
Extract in Lotion and Gel 
The composition of lotion and gel that was used in 
this study are presented in Table 1 and 2. 
The preparations of lotion and gel were 
performed by using fusion principle. The water-
soluble and oil-soluble parts was were soluted in 
water and then heated at a temperature of 70°C. 
Then, the second mixture (water phase) was 
gradually added into the first mixture (oil phase) at 
70°C and was homogenized. The extract of moringa 
was added when it was cold (Munson, 1991). 
2.2.4  Evaluation of Physical Characteristic 
•  Adhesivity test 
The gel or lotion was weighed 0.25 g and then was 
placed between two glass objects. One kilogram of 
load was put on the upper side of glass objects to 
give a tension for 5 minutes. After that, the glass 
object were put on the tool that had 80 grams of 
load. The time was needed for two glass objects 
separated after the load of 80 grams release was 
noted (Putra and Setyawan, 2014). 
•  Spreadability test 
The gel or lotion was weighed 0.5 g and then was 
placed in the middle of a circular glass. The other 
glass was placed on the upper side of it for 1 minute. 
The diameter of lotion or gel was measured. One 
hundred grams of load was placed on the glass for 1 
Table 1: The Formulation of Moringa oleifera leaf 
extract in lotion. 
 
Composition Weight (g)  
Stearic aci